Dendritic Glycerol-Cholesterol Amphiphiles as Drug Delivery Systems: A Comparison between Monomeric and Polymeric Structures

283
0
2023-10-13 15:53
MDPI
PTLv2
Followers:3Columns:927

1. Introduction

Diverse shapes and architectures have been designed as drug delivery systems (DDSs) as an alternative method for anti-cancer drug delivery, aiming to enhance the biocompatibility and tumor targeting that conventional treatments cannot offer [1,2,3]. The ability to transport highly hydrophobic drugs has been another challenge, as delivery systems often show critical issues when interacting with cell membranes [4].

The design of polymeric transport systems from versatile synthetic routes has gained a great deal of attention [5,6], leading to varied architectures such as amphiphilic polymers that are able to self-assemble into polymeric micelles, bilayers, or polymersomes [7,8]. The spontaneous formation of those self-assembled structures relies on the hydrophilic–lipophilic balance (HLB) of the chemical structure, and is observed when the concentration in an aqueous solution is above the critical micelle concentration (CMC) [9].

Recently, a synthetic amphiphilic random copolymer bearing cholesterol moieties (12 wt. %) capable of self-assembly into polymersomes was investigated by Martin et al. [10]. The polymersomes resulted in a ten-fold increase in cellular uptake of dextran into HeLa cells compared to free dextran, improving cellular membrane crossing via endocytosis [10]. The hydroxyl group on the cholesterol structure allows for straightforward synthesis of cholesterol derivatives, with different functional groups usually incorporated into the molecules in two different fashions: either as cholesterol end-capped molecules [11,12] or as chain modified polymers bearing cholesteryl moieties [13,14]. These cholesteryl moieties can be implemented as pendant groups thanks to their high compatibility with anticancer drugs and ability to ameliorate the interaction with the cell membrane as hydrophobic domains of a DDS [4,11,13,15].However, a high concentration of cholesterol-bearing structures shows high cell toxicity; therefore, incorporating the cholesterol with an adjusted HLB ratio can improve the cell viability while enabling the cellular uptake [10]. In this context, a well-defined cholesterol-based “monodisperse” amphiphilic system with precise knowledge about the composition and behavior of biological entities is relevant [16,17]. A great synthetic-route candidate for accomplishing well defined amphiphilic block copolymers is reversible addition–fragmentation chain transfer (RAFT) polymerization [18,19,20,21]. The absence of metal catalysts is an attractive feature of this type of polymerization for biomedical purposes [22,23,24]. In a recent study, a cholesterol end-capped macro-RAFT agent was added to a PNIPAAm backbone to obtain polymeric micelles. The final system did not disrupt red blood cell membranes at concentrations up to 0.25 mg/mL [25].

The prolonged circulation in the blood of micellar systems is mainly a consequence of the physiological behavior of the micelles’ hydrophilic outer shell, which plays a principal role in terms of stability, cellular uptake, and in certain cases reticuloendothelial system (RES) uptake [26,27]. Our group has reported several amphiphilic systems containing polyglycerol (PG) dendrons as hydrophilic parts, which is due to the hydrophilicity and biocompatibility provided to the system by their tree-like structure along with the several terminal hydroxyl groups on the periphery [28,29]. Moreover, their simple chemical structure makes them excellent candidates for incorporation as pendant groups [30]. Recently, Trappmann et al. [31] reported the synthesis of nonionic amphiphilic molecules containing different generations of PG dendrons as hydrophilic parts. These molecules are capable of self-assembly into ring-like, fiber-like, and spherical aggregations for possible application as transport carriers. In another study, nonionic amphiphiles composed of polyglycerol [G2] dendron and single alkyl chains were investigated [32]. The noncytotoxic amphiphilic structures showed superior solubilization properties of hydrophobic molecules than standard excipients used in commercially available surfactant formulations [32].

The aim of this study is to investigate two analogous tailored micellar structures containing PG dendrons as the hydrophilic part and cholesterol moieties as the hydrophobic part (Figure 1). The first structure (left) is an AB-type block copolymer amphiphile synthesized via RAFT polymerization containing poly(G1-polyglycerol dendron methacrylate) and poly(cholesterol methacrylate) blocks. The second structure (right) is a monomeric amphiphile containing a G2-polyglycerol dendron end-capped with one cholesterol unit. In this study, we compare these two structures based on their solubility, size, shape, and cytotoxicity properties. As a proof of concept, the capability of the polymeric structure as a drug carrier is presented as well.

Figure 1. Chemical structure of pG1MAOH-b-pCMA polymeric amphiphiles (left) and G2OH-CHOL monomeric amphiphiles (right).

2. Materials and Methods

Chemicals, materials, and methods are described in detail in .

2.1. Synthesis of Polymeric Amphiphiles

2.2. Synthesis of Monomeric Amphiphiles

2.3. Preparation of Doxorubicin (Free Base)

DOX·HCl (100 mg, 0.172 mmol) was dissolved in 200 mL of water, then Et 3 N (1 mL; 7.2 mmol; 42.0 equiv.) was added. The DOX-free base was extracted three times using chloroform (200 mL). The organic phase was dried over Na 2 SO 4 , the solvent was removed under reduced pressure, and the product was dried overnight under vacuum. The product was obtained in quantitative yield and stored in the freezer. ESI-MS: m/z; calculated: 544.2 g/mol.; found: 544.1 g/mol ([M+H] + ).

2.4. Micelle Formation and Characterization

A suspension of 5 mg of the respective amphiphiles was prepared in a solution mixture of 0.5 mL of acetone (HPLC grade) and 50 μ L of Milli-Q water. The solution was ultrasonicated until no further precipitation was observed. This solution was added dropwise to a vial containing 4.95 mL of Milli-Q water, then acetone was removed under rotary evaporation to obtain micelles with a final concentration of 1 mg/mL. The size and polydispersity index of the micelle solution were recorded by Dynamic Light Scattering (DLS) in low-volume cuvettes at a constant temperature of 37 °C. The ζ -potential was recorded in folded capillary zeta cells at 25 °C. The samples were calibrated for 2 min before each measurement. The critical micelle concentration (CMC) was determined by DLS for pG1MAOH-b-pCMA polymeric micelles and by surface tension for G2OH-CHOL monomeric micelles. DLS studies were performed by observing the derived count rate (in kpcs) at 37 °C for two-folded serial dilutions starting with a concentration of 1 mg/mL of the amphiphiles. The samples were calibrated for 2 min before measurement. Surface tension experiments were recorded in a Dataphysics OCA 20 tensiometer at 25 °C using the pendant drop method. The surface tension of amphiphilic solutions in Milli-Q water was recorded and calculated using the Young–Laplace equation. Samples were vortexed (10 min) and equilibrated 24 h prior to measurement. The surface tension was measured in intervals of 20 s. The experiments were stopped when the surface tension value reached a plateau and did not change for several minutes (in general, after 30–90 min).

2.5. Cryo-Tem Imaging

Perforated carbon film-covered microscopical 200 mesh grids (R1/4 batch of Quantifoil, MicroTools GmbH, Jena, Germany) were cleaned with chloroform and hydrophilized by 60 s glow discharging at 10 mA in a Safematic CCU-010 device (Safematic GmbH, Zizers, Switzerland). Subsequently, 4 μ L aliquots of the sample solution were applied to the grids. The samples were vitrified by automatic blotting and plunge freezing with an FEI Vitrobot Mark IV (Thermo Fisher Scientific Inc., Waltham, MA, USA) using liquid ethane as a cryogen. The vitrified specimens were transferred to the autoloader of an FEI TALOS ARCTICA electron microscope (Thermo Fisher Scientific Inc., Waltham, MA, USA). This microscope is equipped with a high-brightness field-emission gun (XFEG) operated at an acceleration voltage of 200 kV. Micrographs were acquired on an FEI Falcon 3 direct electron detector (Thermo Fisher Scientific Inc., Waltham, MA, USA) using a 100 μm objective aperture. Graphical analysis of the images was performed using Image J v1.53k.

2.6. Encapsulation Studies

Doxorubicin (free base) (DOX) drug was encapsulated in the polymeric micelles by the film method, as described by Prasad et al. [34]. First, a stock solution of DOX was prepared in methanol (C = 1 mg/mL) and 3 mL of drug solution was evaporated under a reduced vacuum forming a film at the bottom of the vial. Then, 20 mL of polymeric micelle solution (C = 1 mg/mL) was added to the vial containing the drug film. The mixture was stirred overnight and filtered through Sephadex G-25 to remove the non-encapsulated drug. The polymeric micelles loaded with DOX were measured by UV-vis at 488 nm. The drug-loading content was calculated from the Lambert–Beer law using a calibration curve of free DOX .

2.7. Cytotoxicity Studies

All cell experiments were conducted according to German genetic engineering laws and German biosafety guidelines in the laboratory (safety level 2).

Cell viability was determined using a Cell Counting Kit-8 (CCK-8 Kit, Sigma; Art. 96992) kit according to the manufacturer’s instructions. A549 cells were obtained from Leibniz-Institut DSMZ—Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH and cultured in Dulbecco’s Modified Eagle Medium (DMEM high glucose GlutaMAX, Gibco; Art. 10566016) supplemented with 10% (v/v) Fetal Bovine Serum (FBS), 100 U/mL penicillin, and 100 μ g/mL streptomycin. A549 cells were routinely cultivated in a 96-well plate at a density of 5 × 10 4 cells/mL in 90 μ L DMEM medium per well overnight at 37 °C and 5% CO 2 until 70% confluency was reached, then subcultured twice a week.

Serial dilutions of the sample in deionized water were prepared; 10 μ L of each sample dilution in serial dilutions, including positive (1% SDS) and negative (DMEM) and solvent (H 2 O) controls, were added and incubated for another 24 h at 37 °C and 5% CO 2 . For background subtraction, wells containing no cells and only samples were used. After 48 h of incubation, the CCK-8 solution was added (10 μ L/well) and the absorbance (450 nm/650 nm) was measured after approximately 3 h incubation of the dye using a Tecan plate reader (SPARK, Tecan Group Ltd., Männedorf, Switzerland). Measurements were performed in technical and biological triplicates. The cell viability was calculated by setting the non-treated control to 100% and the negative control to 0% after subtracting the background signal using Microsoft Excel software v2309. The mean values of all three measurements were plotted and the results were used to determine the half-maximal inhibitory concentration (IC 50 ) using the “log[inhibitor] vs. normalized response (three parameters)” model in GraphPad Prism.

2.8. Cellular Uptake Studies

The cells were propagated as described above. For confocal laser scanning microscopy (CLSM), A549 cells (5 × 10 4 cells/mL) were seeded in eight-well ibidi slides (ibidi treat) in 270 μ L DMEM. After cell attachment for 4–24 h, a post-seeding 30 μ L of the compound-containing solution was added for 20 h. Before imaging, the cells were stained with Hoechst 33342 (1 μ g/mL), washed with PBS, and covered with fresh cell culture medium (DMEM). Confocal images were taken with a Leica DMI6000CSB SP8 inverted confocal laser scanning microscope (Leica, Wetzlar, Germany) with a 63×/1.4 HC PL APO CS2 oil immersion objective using the manufacturer’s provided LAS X software in sequential mode with the following channel settings: Transmission Ch (grey intensity values), excitation laser line 405 nm, detection of transmitted light (photomultiplier); Ch1 (Hoechst 33342): excitation laser line 405 nm, detection range 408–558 nm (hybrid detector); Ch2 (Doxorubicin free base): excitation laser line 561 nm, detection range 564–670 nm (hybrid detector).

3. Results

3.1. Synthesis of Polymeric Amphiphiles

A block copolymer of two methacrylate-based monomers was synthesized by sequential RAFT polymerization, with the expectation of AB-type polymerization of the hydrophobic and hydrophilic blocks. As a building block of the hydrophilic part, the acetal-protected polyglycerol [G1] dendron methacrylate (abbreviated as G1MA monomer) was synthesized via the esterification reaction of the acetal-protected polyglycerol [G1] dendron (G1-OH) and methacryloyl chloride. This dendritic precursor was used in its acetal-protected version to avoid any side reactions or intramolecular transfer of the hydroxyl protons. Deprotection of the acetal groups was performed at the end to achieve the hydrophilic block. As a hydrophobic monomer, cholesterol methacrylate (abbreviated CMA monomer) was synthesized as reported by Zhou et al. [33].

The synthetic route overview of the polymeric structure is depicted in Figure 2A. To synthesize the copolymer, the G1MA monomer was polymerized at the first step using 2-(dodecylthiocarbonothioylthio)-2-methylpropionic acid (abbreviated as DDMAT) as a RAFT agent to obtain the pG1MA homopolymer. The pG1MA was purified by dialysis against acetone and used further as a macro-RAFT agent for the polymerization of the CMA monomer in the presence of a small amount of AIBN, which acted as a co-initiator to obtain the pG1MA-b-pCMAdiblock copolymer. In the end, the acid-catalyzed deprotection of the G1MA block was performed afterward in order to obtain the pG1MAOH-b-pCMA polymeric amphiphiles.

Figure 2. (A) Synthetic route of the pG1MA-b-pCMA block copolymer followed by deprotection of the G1MA block to form pG1MAOH-b-pCMA polymeric amphiphiles. (B) Synthetic route of the G2-CHOL structure followed by deprotection of the G2 dendron to form G2OH-CHOL monomeric amphiphiles.

The homopolymerization of G1MA was monitored by the signal’s shift of the proton adjacent to the ester group from 5.2 ppm to 4.9 ppm in the 1 H NMR spectra of the crude product (Figure A2). A high monomer conversion of 94% was observed from the 1 H NMR of the crude product, as described in . After purification by dialysis, pG1MA homopolymer was characterized by 1 H NMR (Figure 3A) and GPC, the latter showing the targeted molecular weight (M n ≌ 5.0 kDa) and the narrow polydispersity index (Đ ≌ 1.5) of the produced homopolymer (Figure 3B, yellow line).

Figure 3. (A) 1 H NMR of the pG1MA homopolymer. (B) GPC chromatograms of pG1MA homopolymer (yellow) and pG1MA-b-pCMA block copolymer (orange), showing an increase in the M n value from 5.0 to 6.9 kDa. (C) Size distributions (% by volume) from DLS for the pG1MAOH-b-pCMA polymeric micelles (dark blue) and pG1MAOH deprotected homopolymer (light blue) in solution.

pG1MA was used as a macro-RAFT agent in the second step for polymerization of the CMA monomer. Polymerization was carried out with a [macro-RAFT]:[CMA]:[AIBN] molar ratio of 1:6:0.167 in toluene at 65 °C for 20 h and quenched by immersing the reaction flask in liquid nitrogen. The copolymer formation was followed by GPC, observing an increase in the molecular weight from 5 kDa to 6.9 kDa (Figure 3B), resulting in an extent of four cholesterol repeating units to the homopolymer backbone.

The protecting acetal groups from the G1MA block present in the copolymer were hydrolyzed to form the hydrophilic block (Figure 2A). The reaction was acid-catalyzed by dissolving the polymer in methanol, followed by slow dropwise addition of the corresponding amount of hydrochloric acid (37%) to the solution. As a control, deprotection of the pG1MA homopolymer was carried out following the same procedure to obtain hydrophilic pG1MAOH homopolymer.

Figure 4 depicts the 1 H NMR for the polymeric amphiphiles (above) compared to the 1 H NMR spectra of pG1MAOH control (below) in deuterated water. Deprotection was confirmed in both cases based on the disappearance of the acetal-group proton signal at δ = 1.4 ppm. Regarding the polyglycerol [G1] dendron backbone (3.4–4.2 ppm) and the polymer backbone (1–1.5 ppm), both spectra show a similar shape, with a small shift to higher values in the case of the polymeric amphiphiles (see Figure 4 above). Further, in the chemical structure of the polymeric amphiphile (Figure 4 above) it can be noted that the thiocarbonothioyl thio group (marked in the yellow square) is chemically connected to the polycholesterol block. On the contrary, in the pG1MAOH homopolymer structure (Figure 4 below), the sulfur-containing functional group is directly attached to the hydrophilic polyglycerol [G1] dendron block, leading to the small peak observed at 3.3 ppm (the red star). The absence of this peak in the NMR spectra of the polymeric amphiphile suggests successful copolymer formation, in which the peak at 3.3 ppm should not be present.

Figure 4. 1 H NMR in D 2 O of pG1MAOH-b-pcMA polymeric amphiphiles (above) and pG1MAOH control (below). The yellow square highlights the thiocarbonothioyl thio group connected to the hydrophobic polycholesterol block (above) and to the hydrophilic polyglycerol [G1] dendron block (below), leading to the small peak (red star) observed at 3.3 ppm for the latter case.

3.2. Synthesis of Monomeric Amphiphiles

The monomeric amphiphiles consist of the hydrophobic steroidal part of one cholesterol unit in combination with one polyglycerol [G2] dendron unit. For synthesis, the precursor acetal-protected polyglycerol G2-NH 2 dendron (abbreviated G2-NH 2 ) was synthesized as the hydrophilic unit following the previously reported synthetic route [35] in five steps (see ). After purification, the acetal-protected G2-NH 2 dendron was reacted in a single step with the commercially available cholesteryl chloroformate in a base-mediated substitution reaction. The acetal-protected structure was deprotected following the procedure reported by Wyzogrodska et al. [35] to obtain the G2OH-CHOL monomeric amphiphiles. An overview of the synthetic route is shown in Figure 2B.

3.3. Formation and Characterization of Micelles

The polymeric amphiphiles were subjected to nanoprecipitation in aqueous media to investigate their self-assembly behavior. This behavior occurs when the concentration of the amphiphilic block copolymer exceeds the critical micelle concentration (CMC). Above this concentration, the polymeric structure shows an association due to the desired minimal contact with water forming a stable assembly with low free energy, indicating micellar stability [36]. After nanoprecipitation, it is expected that micelle formation will result from the hydrophobic interactions of the cholesterol blocks forming an inner core, minimizing contact with water molecules, with the outer shell composed of the hydrophilic block of the copolymer. DLS was used to investigate the formation of polymeric micelles at a concentration of 1 mg/mL in water. A monomodal size distribution presented a hydrodynamic diameter of around 150 nm by volume. The ζ -potential was measured to be −5 mV, corroborating the formation of a non-ionic polymeric micellar system. The CMC of the polymeric micelles was determined by DLS, observing a value of 0.2 μg/mL .

As a control, the pG1MA homopolymer was deprotected following the same procedure to obtain the hydrophilic homopolymer (abbreviated pG1MAOH). The size distribution of the pG1MAOH control aggregates in water was investigated to compare the impact of adding cholesterol units to the polymer structure. DLS results demonstrated a hydrodynamic diameter of around 100 nm for the pG1MAOH control solution in water at 1 mg/mL (Figure 3C). As expected, a small increase in the hydrodynamic diameter was observed in the case of the copolymer amphiphiles when the cholesterol block was included.

On the other hand, monomeric micelles revealed a CMC of 17.0 μ g/mL as determined by a surface tension experiment , and presented a monomodal size distribution with a hydrodynamic diameter of around 10 nm . Regarding the hydrophilic–lipophilic balance (HLB) of the systems, monomeric and polymeric amphiphiles showed comparable values of 11.3 and 13.6, respectively, calculated as described in . summarizes the characterization results of the pG1MAOH-b-pCMA polymeric micelles and the G2OH-CHOL monomeric micelles.

The morphology of the micellar solutions was observed by cryogenic Transmission Electronic Microscopy (cryo-TEM). The images showed the self-assembly of the polymeric micelles into spherical aggregations, as shown in Figure 5A1,A2. The diameters of 100 particles were determined and found to be approximately 80 nm (Figure 5A3), corresponding to the typical values of non-ionic polymeric micelles [7]. In the case of the monomeric micelles, small and well-distributed spherical micelles were identified, as shown in Figure 5B1,B2. Similarly, the diameters of 100 particles were determined and found to be around 6 nm (Figure 5B3), showing similar values to other non-ionic dendritic polyglycerol amphiphilic structures [37]. This indicates that the spherical particles are likely composed of a small number of self-assembled amphiphiles [38].

Figure 5. Cryo-TEM micrographs of pG1MAOH-b-pCMA polymeric micelles at (A1) 28,000× and (A2) 45,000× magnification and G2OH-CHOL monomeric micelles at (B1) 58,300× magnification and (B2) digital zoom; histograms of 100-micelle size from the analysis of cryo-TEM images of (A3) polymeric micelles and (B3) monomeric micelles.

In both cases, the diameters of the particles observed by cryo-TEM were smaller compared to the DLS measurements. This decrease in size can be explained by the differences between the two methods. DLS measures the hydrodynamic diameter is measured, which means that the particles’ hydration shell is considered. On the other hand, the hydration shell is not visualized in cryo-TEM experiments; therefore, smaller diameters were obtained for the micelles.

3.4. Cell Viability

A preliminary assessment of cytotoxicity (Figure 6) was carried out via CCK-8 Kit assays on A549 cells treated with empty polymeric micelles (blue) and monomeric micelles (green). Ten-fold serial dilutions of the samples were prepared in both cases, starting with 1000 μ g/mL micellar solution. As revealed by Figure 6, the monomeric micelles show a severe cytotoxic effect, with less than 10% viable cells at 1000 μ g/mL and up to 75% viable cells for a concentration of 10 μ g/mL, which is considered very low for employment in biological systems and is below the CMC value (17 μ g/mL). According to the literature, the toxic effect of excess cellular free cholesterol results mainly from two protective mechanisms against its accumulation, namely, cholesterol esterification and cellular efflux of cholesterol, and may be due to certain cholesterol-derived oxysterols as well [39]. Thus, the toxic effect of the monomeric micelles can be attributed to the fact that the polyglycerol [G2] dendron end-capped with cholesterol molecules can be inserted into cell membranes following a similar mechanism as free cholesterol [40], resulting in low viability of the treated cells. On the other hand, the polymeric micelles reveal 80% cell viability after 48 h even at high concentrations (1000 μ g/mL).

Figure 6. Cell viability of A549 cells treated with polymeric micelles (blue), monomeric micelles (green), and control (light orange). Each bar represents the mean of three independent experiments with the standard deviation.

3.5. Characterization and In Vitro Studies of DOX-Loaded Polymeric Micelles

The good biocompatibility of the polymeric micelles led us to investigate their efficacy as drug carriers by encapsulating DOX (free base) as a drug model. Here, a hydrophobic interaction between the cholesterol block and the drug was expected to be the driving force of drug loading. The micelles were loaded with 20 wt% of the drug and purified before characterization. The loading capacity (LC) and encapsulation efficiency (EE) of the micelles were calculated as stated in . The polymeric micellar system showed a loading capacity of 4% and an encapsulation efficiency of 14%. DLS characterization of the DOX-loaded micellar solution revealed a monomodal particle distribution with a slightly smaller hydrodynamic diameter of loaded micelles (140 nm) compared to empty micelles (around 150 nm). The shrinking behavior of the encapsulated system could be due to the hydrophobic host–drug interaction. Further, cryo-TEM micrographs of the DOX-loaded polymeric micelles were investigated, where a spherical micellar shape was again observed . These results show that there is no significant impact on size and morphology after the encapsulation of doxorubicin in the polymeric micelles. The viability of A549 cells treated with DOX-loaded polymeric micelles was compared to non-loaded polymeric micelles and free DOX to inspect the possibility of DOX being released from the micelles and promoting cell death. Therefore, the IC 50 values were determined through plot fitting using a nonlinear regression model (inhibitor) vs. the normalized response, first for the non-loaded and DOX-loaded micelles based on the polymeric micelles concentration (Figure 7A), and then for the DOX-loaded micelles and free DOX based on DOX concentration (Figure 7B). Based on the micelles concentration, the IC 50 of the empty micelles was 1555.0 μ g/mL, in comparison to 264.5 μ g/mL for the loaded ones, indicating that the DOX-containing micelles are indeed more toxic than the empty micelles. Based on the free DOX concentration, the DOX-loaded in the micelles had an IC 50 of 5.3 μ g/mL, while the IC 50 of free DOX was 9.8 μ g/mL. This implies that DOX might be effectively encapsulated, solubilized, and sustainably released from the micelles and that the encapsulation does not affect the activity of the drug or its effect on the cells. The IC 50 values are summarized in .

Figure 7. Cell viability of A549 cells after 48 h treatment with (A) empty polymeric micelles (blue) and DOX-loaded polymeric micelles (red) based on polymeric micelle concentration, and (B) DOX-loaded polymeric micelles (red) and free DOX (pink) based on DOX concentration. Each point represents the mean of three independent experiments with the standard deviation.

Confocal laser scanning microscopy (CLSM) was used to monitor the cellular uptake of living A549 cells after 20 h treatment with the DOX-loaded and empty polymeric micelles as well as the uptake of free DOX after incubation. The red fluorescence observed in the cell nucleus treated with DOX-loaded polymeric micelles (Figure 8A) suggests that free doxorubicin was released from the polymeric micelles, taken up inside the cells, and mainly distributed in the cytoplasm and within the nuclei, as the polymeric micelles are too large (d H = 145 nm) to enter the nucleus. Additionally, the red fluorescence of cells treated with DOX-loaded polymeric micelles (Figure 8A) is qualitatively more intense than free DOX (Figure 8C) at the same tested concentration of DOX (2%), suggesting enhanced uptake by A459 cells and an improvement in the bioavailability of doxorubicin (free base).

Figure 8. Confocal Laser Scanning Microscopy (CLSM) images of A549 cells treated for 20 h with (A) DOX-loaded polymeric micelles (100 μg/mL polymeric micelles + 2% DOX formulation), (B) empty polymeric micelles (100 μg/mL), and (C) free DOX (2 μg/mL). (D) Non-treated cells served as a control. Blue shows Hoechst staining in the nuclei, while red shows DOX. For all images, the scale bar represents 5 μm.

4. Discussion

Herein, we have employed RAFT polymerization to synthesize well-defined non-ionic polymeric amphiphiles composed of polyglycerol dendrons as the hydrophilic block and polycholesterol as the hydrophobic block. The amphiphiles are capable of self-assembly behavior, as confirmed by cryo-TEM images. The micelle diameter was around 80 nm as measured by cryo-TEM, and the hydrodynamic diameter was 150 nm as measured by DLS. In addition, a polyglycerol–cholesterol monomeric structure was synthesized with a similar hydrophilic–lipophilic balance on the part of the polymeric amphiphiles. Their morphology was observed by cryo-TEM, revealing smaller spherical micelles of 6 nm in diameter, while the hydrodynamic size was shown to be 10 nm by DLS measurement. The CMC of both systems was detected in a typical micellar range of 0.1–10 mg/L. As a proof of concept, the polymeric micelles were tested as possible drug carriers, using doxorubicin as a hydrophobic drug model. The obtained loading capacity was 4%, while the morphology and the hydrodynamic size remained similar to those of empty carriers.

The cytotoxicity studies of the polymeric micelles using the A549 cell line suggest good biocompatibility up to relatively high concentrations (1000 μ g/mL). In comparison, the monomeric micelles revealed a severe cytotoxic effect at the same concentration, suggesting that monomeric micelles may penetrate the cell membrane by following a mechanism similar to free cholesterol. On the other hand, the presented polymeric micelles combine a low CMC (0.2 μ g/mL) and a highly tested biocompatible concentration (1000 μ g/mL), suggesting a broad safe window of micellar concentrations for application as a biocompatible drug delivery system. The cellular uptake of the DOX-loaded polymeric micelles was examined via confocal laser scanning microscopy. Our observations indicated that the carriers are taken up efficiently by A549 cells, showing a possible sustained release of doxorubicin, as indicated by the accumulation of DOX in the cell nucleus.

All of these properties, together with the incorporation of cholesterol as pendant groups in the design of a polymeric structure, suggest a promising method of preparation for efficient drug delivery systems while improving the cell toxicity of the monomeric cholesterol structure.

References

  1. Pucci, C.; Martinelli, C.; Ciofani, G. Innovative approaches for cancer treatment: Current perspectives and new challenges. Ecancer 2019, 13, 961. [Google Scholar] [CrossRef] [PubMed]
  2. Shi, J.; Votruba, A.R.; Farokhzad, O.C.; Langer, R. Nanotechnology in drug delivery and tissue engineering: From discovery to applications. Nano Lett. 2010, 10, 3223–3230. [Google Scholar] [CrossRef] [PubMed]
  3. Dagogo-Jack, I.; Shaw, A.T. Tumour heterogeneity and resistance to cancer therapies. Nat. Rev. Clin. Oncol. 2018, 15, 81–94. [Google Scholar] [CrossRef] [PubMed]
  4. Zhang, R.; Qin, X.; Kong, F.; Chen, P.; Pan, G. Improving cellular uptake of therapeutic entities through interaction with components of cell membrane. Drug Deliv. 2019, 26, 328–342. [Google Scholar] [CrossRef] [PubMed]
  5. Liechty, W.B.; Kryscio, D.R.; Slaughter, B.V.; Peppas, N.A. Polymers for drug delivery systems. Annu. Rev. Chem. Biomol. Eng. 2010, 1, 149–173. [Google Scholar] [CrossRef] [PubMed]
  6. Kumari, P.; Ghosh, B.; Biswas, S. Nanocarriers for cancer-targeted drug delivery. J. Drug Target. 2016, 24, 179–191. [Google Scholar] [CrossRef] [PubMed]
  7. Xu, W.; Ling, P.; Zhang, T. Polymeric Micelles, a Promising Drug Delivery System to Enhance Bioavailability of Poorly Water-Soluble Drugs. J. Drug Deliv. 2013, 2013, 340315. [Google Scholar] [CrossRef] [PubMed]
  8. Zhang, X.y.; Zhang, P.y. Polymersomes in Nanomedicine—A Review. Curr. Nanosci. 2016, 13, 124–129. [Google Scholar] [CrossRef]
  9. Nagarajan, R.; Ganesh, K. Block copolymer self-assembly in selective solvents: Spherical micelles with segregated cores. J. Chem. Phys. 1989, 90, 5843–5856. [Google Scholar] [CrossRef]
  10. Martin, C.; Marino, N.; Curran, C.; McHale, A.P.; Callan, J.F.; Callan, B. Cholesteryl to improve the cellular uptake of polymersomes within HeLa cells. Int. J. Pharm. 2016, 511, 570–578. [Google Scholar] [CrossRef]
  11. Kumari, P.; Muddineti, O.S.; Rompicharla, S.V.K.; Ghanta, P.; Adithya, K.B.; Ghosh, B.; Biswas, S. Cholesterol-conjugated poly(D, L-lactide)-based micelles as a nanocarrier system for effective delivery of curcumin in cancer therapy. Drug Deliv. 2017, 24, 209–223. [Google Scholar] [CrossRef] [PubMed]
  12. Song, Y.; Tian, Q.; Huang, Z.; Fan, D.; She, Z.; Liu, X.; Cheng, X.; Yu, B.; Deng, Y. Self-assembled micelles of novel amphiphilic copolymer cholesterol-coupled F68 containing cabazitaxel as a drug delivery system. Int. J. Nanomed. 2014, 9, 2307–2317. [Google Scholar] [CrossRef]
  13. Lee, A.L.; Venkataraman, S.; Sirat, S.B.; Gao, S.; Hedrick, J.L.; Yang, Y.Y. The use of cholesterol-containing biodegradable block copolymers to exploit hydrophobic interactions for the delivery of anticancer drugs. Biomaterials 2012, 33, 1921–1928. [Google Scholar] [CrossRef]
  14. Misiak, P.; Markiewicz, K.H.; Szymczuk, D.; Wilczewska, A.Z. Polymeric drug delivery systems bearing cholesterol moieties: A review. Polymers 2020, 12, 2620. [Google Scholar] [CrossRef] [PubMed]
  15. Tran, T.H.; Nguyen, C.T.; Gonzalez-Fajardo, L.; Hargrove, D.; Song, D.; Deshmukh, P.; Mahajan, L.; Ndaya, D.; Lai, L.; Kasi, R.M.; et al. Long Circulating Self-Assembled Nanoparticles from Cholesterol-Containing Brush-Like Block Copolymers for Improved Drug Delivery to Tumors. Biomacromolecules 2014, 15, 4363–4375. [Google Scholar] [CrossRef] [PubMed]
  16. Thunemann, A.F.; Gruber, A.; Klinger, D. Amphiphilic Nanogels: Fuzzy Spheres with a Pseudo-Periodic Internal Structure. Langmuir 2020, 36, 10979–10988. [Google Scholar] [CrossRef] [PubMed]
  17. Wan, Q.; Huang, B.; Li, T.; Xiao, Y.; He, Y.; Du, W.; Wang, B.Z.; Dakin, G.F.; Rosenbaum, M.; Goncalves, M.D.; et al. Selective targeting of visceral adiposity by polycation nanomedicine. Nat. Nanotechnol. 2022, 17, 1311–1321. [Google Scholar] [CrossRef] [PubMed]
  18. Perrier, S. 50th Anniversary Perspective: RAFT Polymerization—A User Guide. Macromolecules 2017, 50, 7433–7447. [Google Scholar] [CrossRef]
  19. He, S.J.; Zhang, Y.; Cui, Z.H.; Tao, Y.Z.; Zhang, B.L. Controlled radical polymerization of cholesteryl acrylate and its block copolymer with styrene via the RAFT process. Eur. Polym. J. 2009, 45, 2395–2401. [Google Scholar] [CrossRef]
  20. Keddie, D.J. A guide to the synthesis of block copolymers using reversible-addition fragmentation chain transfer (RAFT) polymerization. Chem. Soc. Rev. 2014, 43, 496–505. [Google Scholar] [CrossRef] [PubMed]
  21. Magami, S.M.; Abdulganiyyu, U. Raft approach to the copolymerisation of methyl methacrylate based polymeric micelles. Bayero J. Pure Appl. Sci. 2017, 10, 197. [Google Scholar] [CrossRef]
  22. Semsarilar, M.; Perrier, S. ’Green’ reversible addition-fragmentation chain-transfer (RAFT) polymerization. Nat. Chem. 2010, 2, 811–820. [Google Scholar] [CrossRef] [PubMed]
  23. Boyer, C.; Bulmus, V.; Davis, T.P.; Ladmiral, V.; Liu, J.; Perrier, S. Bioapplications of RAFT polymerization. Chem. Rev. 2009, 109, 5402–5436. [Google Scholar] [CrossRef] [PubMed]
  24. Moad, G.; Rizzardo, E.; Thang, S.H. Living radical polymerization by the RAFT process—A second update. Aust. J. Chem. 2009, 62, 1402–1472. [Google Scholar] [CrossRef]
  25. Misiak, P.; Niemirowicz- Laskowska, K.; Markiewicz, K.H.; Misztalewska-Turkowicz, I.; Wielgat, P.; Kurowska, I.; Siemiaszko, G.; Destarac, M.; Car, H.; Wilczewska, A.Z. Evaluation of cytotoxic effect of cholesterol end-capped poly(N-isopropylacrylamide)s on selected normal and neoplastic cells. Int. J. Nanomed. 2020, 15, 7263–7278. [Google Scholar] [CrossRef] [PubMed]
  26. Adams, M.L.; Lavasanifar, A.; Kwon, G.S. Amphiphilic block copolymers for drug delivery. J. Pharm. Sci. 2003, 92, 1343–1355. [Google Scholar] [CrossRef]
  27. Yoncheva, K.; Calleja, P.; Agüeros, M.; Petrov, P.; Miladinova, I.; Tsvetanov, C.; Irache, J.M. Stabilized micelles as delivery vehicles for paclitaxel. Int. J. Pharm. 2012, 436, 258–264. [Google Scholar] [CrossRef] [PubMed]
  28. Prasad, S.; Achazi, K.; Böttcher, C.; Haag, R.; Sharma, S.K. Fabrication of nanostructures through self-assembly of non-ionic amphiphiles for biomedical applications. RSC Adv. 2017, 7, 22121–22132. [Google Scholar] [CrossRef]
  29. Rodrigo, A.C.; Malhotra, S.; Böttcher, C.; Adeli, M.; Haag, R. Dendritic polyglycerol cyclodextrin amphiphiles and their self-assembled architectures to transport hydrophobic guest molecules. RSC Adv. 2014, 4, 61656–61659. [Google Scholar] [CrossRef]
  30. Haag, R.; Kratz, F. Polymer therapeutics: Concepts and applications. Angew. Chem.-Int. Ed. 2006, 45, 1198–1215. [Google Scholar] [CrossRef]
  31. Trappmann, B.; Ludwig, K.; Radowski, M.R.; Shukla, A.; Mohr, A.; Rehage, H.; Böttcher, C.; Haag, R. A new family of nonionic dendritic amphiphiles displaying unexpected packing parameters in micellar assemblies. J. Am. Chem. Soc. 2010, 132, 11119–11124. [Google Scholar] [CrossRef]
  32. Richter, A.; Wiedekind, A.; Krause, M.; Kissel, T.; Haag, R.; Olbrich, C. Non-ionic dendritic glycerol-based amphiphiles: Novel excipients for the solubilization of poorly water-soluble anticancer drug Sagopilone. Eur. J. Pharm. Sci. 2010, 40, 48–55. [Google Scholar] [CrossRef] [PubMed]
  33. Zhou, Y.; Kasi, R.M. Synthesis and Characterization of Polycholesteryl Methacrylate–Polyhydroxyethyl Methyacrylate Block Copolymers. J. Polym. Sci. Part A Polym. Chem. 2008, 46, 6801–6809. [Google Scholar] [CrossRef]
  34. Prasad, S.; Achazi, K.; Schade, B.; Haag, R.; Sharma, S.K. Nonionic Dendritic and Carbohydrate Based Amphiphiles: Self-Assembly and Transport Behavior. Macromol. Biosci. 2018, 18, 1800019. [Google Scholar] [CrossRef] [PubMed]
  35. Wyszogrodzka, M.; Haag, R. A convergent approach to biocompatible polyglycerol "click" dendrons for the synthesis of modular core-shell architectures and their transport behavior. Chem.-Eur. J. 2008, 14, 9202–9214. [Google Scholar] [CrossRef]
  36. Patravale, V.B.; Upadhaya, P.G.; Jain, R.D. Preparation and Characterization of Micelles; Humana Press Inc.: Totowa, NJ, USA, 2019; Volume 2000, pp. 19–29. [Google Scholar] [CrossRef]
  37. Rashmi; Singh, A.K.; Achazi, K.; Schade, B.; Böttcher, C.; Haag, R.; Sharma, S.K. Synthesis of non-ionic bolaamphiphiles and study of their self-assembly and transport behaviour for drug delivery applications. RSC Adv. 2018, 8, 31777–31782. [Google Scholar] [CrossRef] [PubMed]
  38. Tschiche, A.; Staedtler, A.M.; Malhotra, S.; Bauer, H.; Böttcher, C.; Sharbati, S.; Calderón, M.; Koch, M.; Zollner, T.M.; Barnard, A.; et al. Polyglycerol-based amphiphilic dendrons as potential siRNA carriers for in vivo applications. J. Mater. Chem. B 2014, 2, 2153–2167. [Google Scholar] [CrossRef]
  39. Tabas, I. Consequences of cellular cholesterol accumulation: Basic concepts and physiological implications. J. Clin. Investig. 2002, 110, 905–911. [Google Scholar] [CrossRef]
  40. Krause, M.R.; Regen, S.L. The Structural Role of Cholesterol in Cell Membranes: From Condensed Bilayers to Lipid Rafts. Accounts Chem. Res. 2014, 47, 3512–3521. [Google Scholar] [CrossRef] [PubMed]
  41. Alpugan, S.; Garcia, G.; Poyer, F.; Durmuş, M.; Maillard, P.; Ahsen, V.; Dumoulin, F. Dendrimeric-like hexadecahydroxylated zinc phthalocyanine. J. Porphyrins Phthalocyanines 2013, 17, 596–603. [Google Scholar] [CrossRef]
  42. Griffin, W.C. Calculation of HLB values of non-ionic surfactants. J. Soc. Cosmet. Chem. 1954, 5, 249–256. [Google Scholar]
Related Suggestion
Remote Loading: The Missing Piece for Achieving High Drug Payload and Rapid Release in Polymeric Microbubbles
Technology
The use of drug-loaded microbubbles for targeted drug delivery, particularly in cancer treatment, has been extensively studied in recent years. However, the loading capacity of microbubbles has been limited due to their surface area. Typically, drug molecules are loaded on or within the shell, or drug-loaded nanoparticles are coated on the surfaces of microbubbles. To address this significant limitation, we have introduced a novel approach. For the first time, we employed a transmembrane ammonium sulfate and pH gradient to load doxorubicin in a crystallized form in the core of polymeric microcapsules. Subsequently, we created remotely loaded microbubbles (RLMBs) through the sublimation of the liquid core of the microcapsules. Remotely loaded microcapsules exhibited an 18-fold increase in drug payload compared with physically loaded microcapsules. Furthermore, we investigated the drug release of RLMBs when exposed to an ultrasound field. After 120 s, an impressive 82.4 ± 5.5% of the loaded doxorubicin was released, demonstrating the remarkable capability of remotely loaded microbubbles for on-demand drug release. This study is the first to report such microbubbles that enable rapid drug release from the core. This innovative technique holds great promise in enhancing drug loading capacity and advancing targeted drug delivery.
356
0
Dual-Ligand Synergistic Targeting Anti-Tumor Nanoplatforms with Cascade-Responsive Drug Release
Technology
Dual-ligand targeting drug delivery nanoplatforms are considered a promising tool for enhancing the specificity of chemotherapy. However, serious off-target delivery has been observed in current dual-ligand targeting nanoplatforms, as each ligand can independently recognize receptors on the cell membrane surface and guide drug nanocarriers to different cells. To overcome this barrier, a dual-ligand synergistic targeting (DLST) nanoplatform is developed, which can guide chemotherapy treatment specifically to cancer cells simultaneously overexpressing two receptors. This nanoplatform consists of a singlet oxygen (1O2) photosensitizer-loaded nanocarrier and a drug-loaded nanocarrier with 1O2 responsiveness, which were, respectively, decorated with a pair of complementary DNA sequences and two different ligands. For cancer cells overexpressing both receptors, two nanocarriers can be internalized in larger quantities to cause DNA hybridization-induced nanocarrier aggregation, which further activates 1O2-triggered drug release under light irradiation. For cells overexpressing a single receptor, only one type of nanocarrier can be internalized in a large quantity, leading to blocked drug release due to the ultrashort action radius of 1O2. In vivo evaluation showed this DLST nanoplatform displayed highly specific tumor treatment with minimized long-term toxicity. This is a highly efficient drug delivery system for DLST chemotherapy, holding great potential for clinical applications.
248
0
Variations in the Relative Abundance of Gut Bacteria Correlate with Lipid Profiles in Healthy Adults
Technology
The gut microbiome is a versatile system regulating numerous aspects of host metabolism. Among other traits, variations in the composition of gut microbial communities are related to blood lipid patterns and hyperlipidaemia, yet inconsistent association patterns exist. This study aims to assess the relationships between the composition of the gut microbiome and variations in lipid profiles among healthy adults. This study used data and samples from 23 adult participants of a previously conducted dietary intervention study. Circulating lipid measurements and whole-metagenome sequences of the gut microbiome were derived from 180 blood and faecal samples collected from eight visits distributed across an 11-week study. Lipid-related variables explained approximately 4.5% of the variation in gut microbiome compositions, with higher effects observed for total cholesterol and high-density lipoproteins. Species from the genera Odoribacter, Anaerostipes, and Parabacteroides correlated with increased serum lipid levels, whereas probiotic species like Akkermansia muciniphila were more abundant among participants with healthier blood lipid profiles. An inverse correlation with serum cholesterol was also observed for Massilistercora timonensis, a player in regulating lipid turnover. The observed correlation patterns add to the growing evidence supporting the role of the gut microbiome as an essential regulator of host lipid metabolism.
43
0
Comments 0
Please to post a comment~
Loading...
Likes
Send-Pen
Favorites
Comment