Thermal properties and physicochemical behavior in aqueous solution of pyrene-labeled poly(ethylene glycol)-polylactide conjugate
Received 27 January 2015
Accepted for publication 5 March 2015
Published 8 April 2015 Volume 2015:10(1) Pages 2815—2822
Checked for plagiarism Yes
Review by Single anonymous peer review
Peer reviewer comments 4
Editor who approved publication: Dr Thomas Webster
Wei-Lin Chen,1,2 Yun-Fen Peng,1,3 Sheng-Kuo Chiang,1 Ming-Hsi Huang1–3
1National Institute of Infectious Diseases and Vaccinology, National Health Research Institutes, Miaoli, Taiwan; 2Graduate Institute of Life Sciences, National Defense Medical Center, Taipei, Taiwan; 3PhD Program in Tissue Engineering and Regenerative Medicine, National Chung Hsing University, Taichung, Taiwan
Abstract: A fluorescence-labeled bioresorbable polymer was prepared by a coupling reaction of poly(ethylene glycol)-polylactide (PEG-PLA) with carboxyl pyrene, using N,N’-diisopropylcarbodiimide/1-hydroxy-7-azabenzotriazole (DIC/HOAt) as a coupling agent and 4-dimethylaminopyridine (DMAP) as a catalyst. The obtained copolymer, termed PEG-PLA-pyrene, was characterized using various analytical techniques, such as gel permeation chromatography (GPC), matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), proton nuclear magnetic resonance (1H-NMR), infrared spectroscopy (IR), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA), to identify the molecular structure and to monitor the thermal property changes before and after the reaction. The presence of a pyrene moiety at the end of polylactide (PLA) did not alter the crystallization ability of the poly(ethylene glycol) (PEG) blocks, indicating that the conjugate preserved the inherent thermal properties of PEG-PLA. However, the presence of PEG-PLA blocks strongly reduced the melting of pyrene, indicating that the thermal characteristics were sensitive to PEG-PLA incorporation. Regarding the physicochemical behavior in aqueous solution, a higher concentration of PEG-PLA-pyrene resulted in a higher ultraviolet-visible (UV-vis) absorbance and fluorescence emission intensity. This is of great interest for the use of this conjugate as a fluorescence probe to study the in vivo distribution as well as the internalization and intracellular localization of polymeric micelles.
Keywords: bioresorbable polymer, fluorescence probe, pyrene, polymeric micelles, poly (ethylene glycol)-polylactide, PEG-PLA
Amphiphilic block copolymers of poly(ethylene glycol) (PEG) and polylactide (PLA) have attracted substantial attention for the sustained delivery of biologically active agents due to their biocompatibility and bioresorbability.1–7 Studies have been performed to investigate the degradability and permeability of PEG/PLA-based vehicles, such as hydrogels,1,2 micelles,3,4 micro/nanoparticles,5 and emulsions,6,7 among others. Ideally, a bioresorbable delivery vehicle must degrade and resorb in vivo at a predefined rate, allowing the bioactive agents to either attach at the surface or be entrapped within the microenvironment before administration and be sequentially released postadministration.1–3,5–7 Attempts have been made to investigate the in vivo distribution, to elucidate the targeting delivery of bioactive candidates bearing fluorescence.5,8 Moreover, understanding the internalization and intracellular localization of the bioactive candidates after formulation with these types of vehicles is useful to elucidate the biological interactions and the mechanism of enhanced therapeutic efficacy of the targeted delivery.
Pyrene and its derivatives have been widely used as fluorescence probes and as models of drugs with poor water solubility.8–11 Due to pyrene’s polycyclic aromatic structure, it is highly stable, with a high quantum yield and lifetime.11 In this study, we report the synthesis of a PEG-PLA copolymer bearing a fluorescence marker, obtained by ring-opening polymerization of DL-lactide in the presence of monomethoxy PEG followed by the coupling reaction with carboxyl pyrene. The obtained PEG-PLA-pyrene copolymer was characterized by gel permeation chromatography (GPC), matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF MS), proton nuclear magnetic resonance (1H-NMR), infrared spectroscopy (IR), differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The physicochemical behavior of PEG-PLA-pyrene in aqueous solution was investigated by ultraviolet (UV)–visible (vis) absorption spectroscopy, fluorescence spectroscopy, and dynamic light scattering (DLS) technology. The results were compared with those obtained from different polymer precursors as described in the literature.4,8
Materials and methods
DL-lactide was purchased from Sigma-Aldrich Corp (St Louis, MO, USA) and was recrystallized from ethyl acetate. Polyethylene glycol 2000 monomethyl ether (MePEG2000) was supplied by Fluka (Buchs, Switzerland) and was used as received. Tin(II) 2-ethylhexanoate (SnOct2), deuterated chloroform, α-cyano-4-hydroxycinnamic acid (CHCA), and sodium trifluoroacetate (Na-TFA) were purchased from Sigma-Aldrich Corp. 1-Pyrenebutyric acid was purchased from Alfa Aesar (Ward Hill, MA, USA). N,N’-diisopropylcarbodiimide (DIC), 1-hydroxy-7-azabenzotriazole (HOAt), and 4-dimethylaminopyridine (DMAP) were purchased from Merck KGaA (Darmstadt, Germany). All of the solvents were of analytical grade.
The AB-type diblock copolymer PEG-PLA was synthesized by ring-opening polymerization of DL-lactide in the presence of MePEG2000 and SnOct2, as previously described.7 In a typical synthesis, DL-lactide (4 g), MePEG2000 (8 g), and SnOct2 (30 mg) were introduced into a round-bottomed flask. Polymerization was performed under vacuum at 140°C for 24 hours. The obtained polymer was recovered by the dissolution/precipitation method, with acetone as the solvent and ethanol as the nonsolvent, followed by filtration and vacuum drying. The coupling reaction of PEG-PLA and 1-pyrenebutyric acid was performed with HOAt/DIC/DMAP in N-methyl-2-pyrrolidone at room temperature for 10 hours. The resulting PEG-PLA-pyrene was recovered by the precipitation method, with diethyl ether as the nonsolvent.
GPC was performed by using a setting composed of an isocratic pump, a refractive index detector, and two size-exclusion columns connected in series, one PLgel™ 5 μm guard column (7.5×50 mm), and one PLgel 5 μm mixed-D column (7.5×300 mm). The mobile phase was tetrahydrofuran, and the flow rate was 1.0 mL·min−1. The data were expressed relative to polystyrene standards (Varian Inc., Amherst, MA, USA). Mass spectra were acquired using a Micromass® MALDI micro MX™ Time of Flight Mass Spectrometer (Waters®, Milford, MA, USA) in the reflection mode. An aliquot (1 μL) of polymer samples was premixed with 1 μL of 0.2% trifluoroacetic acid/acetonitrile and then mixed with CHCA as the matrix and Na-TFA as the dopant. An aliquot (1 μL) of sample solutions was spotted on a MALDI sample plate and air-dried to form a thin matrix/analyte film. 1H-NMR spectra were recorded at room temperature with a Varian VXR 300 MHz spectrometer using deuterated chloroform as the solvent and tetramethylsilane as the shift reference. IR spectra were recorded with a PerkinElmer Spectrum 100 FTIR Spectrometer (PerkinElmer, Santa Clara, CA, USA). DSC and TGA measurements were obtained on a SDT Q600 thermal analyzer (TA Instruments, New Castle, DE, USA) under nitrogen at a heating rate of 10°C·min−1. The polymeric micellar solutions in distilled water were incubated in 96-well quartz microplates. The absorbance and fluorescence measurements of the samples were obtained on a SpectraMax® M2 multimode plate reader (Molecular Devices LLC., Sunnyvale, CA, USA). The absorbance spectra were recorded from 300 to 600 nm with a width of 10 nm. The fluorescence was measured using an excitation wavelength of 340 nm, and the excitation and emission slits were 10 nm wide. The particle size of the polymer in aqueous solution was monitored by DLS technique (Brookhaven 90Plus Particle Size Analyzer, Brookhaven Instruments Corp, Holtsville, NY, USA).
Results and discussion
The schematic diagrams of the synthesis and the chemical structure of the block copolymers are shown in Figure 1. The PEG-PLA diblock copolymer was synthesized by ring-opening polymerization of DL-lactide on monomethoxy PEG, resulting in an AB-type copolymer composed of a hydrophilic block of PEG and a lipophilic block of PLA, with a methoxy group at the PEG terminal and a hydroxyl group at the PLA end. PEG-PLA-pyrene was synthesized by coupling PEG-PLA with a carboxyl pyrene and 1-pyrenebutyric acid, using DIC/HOAt as a coupling agent and DMAP as the catalyst. Table 1 summarizes the molecular characteristics of 1-pyrenebutyric acid, PEG-PLA, and PEG-PLA-pyrene.
Figure 2A presents the GPC traces of PEG-PLA-pyrene, PEG-PLA, and the corresponding fluorescence labeling reagent carboxyl pyrene. PEG-PLA-pyrene exhibited a single peak with a narrow molecular weight distribution, indicating the absence of unreacted 1-pyrenebutyric acid. MALDI-TOF MS was used to measure the detailed molecular weight of the pyrene-labeled PEG-PLA block copolymer. As shown in Figure 2B, the PEG-PLA spectra were well-resolved, and the peaks were separated by 44 and 72 mass units, which corresponded to the molecular weight of the OE motif (oxyethylene units =44.03 g·mol−1) and LA motif (lactyl units =72.06 g·mol−1), respectively. The molecular weight of PEG-PLA ranged from 1,500 to 2,800 g·mol−1. After coupling with 1-pyrenebutyric acid, the molecular weight distribution of the resulting polymer shifted to 1,800–3,200 g·mol−1, which indicated the chain extension of the pyrene moiety onto PEG-PLA. Figure 2C shows the 1H-NMR spectrum of the PEG-PLA-pyrene block copolymer in deuterated chloroform. Typical signals of the PLA and PEG components were observed, as follows: signals at 1.5 (–CH3) and 5.2 ppm (–CH) were assigned to PLA blocks and the signal at 3.6 ppm (–CH2–) to PEG blocks.2 The coupling of pyrene was confirmed by the appearance of an aromatic proton peak area between 7.8 and 8.6 ppm4, and the absence of a peak at 12.2 ppm (–OH) for the starting carboxyl pyrene. The PEG/PLA weight ratio of PEG-PLA-pyrene (~25 wt% PLA content) was determined from the integrations of the signals due to PEG blocks at 3.6 ppm and to PLA blocks at 1.5 ppm. The same method was used to calculate the pyrene/PEG-PLA ratio (the molar ratio of pyrene conjugated to the PEG-PLA chain) was about 70%, from the ratio of the area of PLA resonances at 1.5 ppm to the area of pyrene resonances between 7.8 and 8.6 ppm. Figure 2D shows the IR spectra of 1-pyrenebutyric acid, PEG-PLA, and the corresponding PEG-PLA-pyrene. 1-Pyrenebutyric acid exhibited bands at 3,052 and 1,694 cm−1 due to OH and C=O stretching of carboxylic acid groups, and the band at 847 cm−1 was due to aromatic stretching.12 On the PEG-PLA spectrum, the bands at 2,885 and 1,118 cm−1 were assigned to C–H and C–O–C stretching, and those at 947 and 844 cm−1 were due to the crystalline phase of PEG.13 Another C–O stretching band appeared at 1,757 cm−1, in agreement with the presence of PLA blocks.13 On the PEG-PLA-pyrene spectrum, the stretching vibration of the conjugated C=O group shifted to 1,645 cm−1, in agreement with the presence of carboxyl pyrene. Moreover, the OH stretching peak of 1-pyrenebutyric acid at 3,052 cm−1 disappeared in the PEG-PLA-pyrene spectrum, which proved the complete esterification reaction of fluorescence probe labeling.
Studies have been performed to prepare PLA-pyrene or PEG-PLA-pyrene conjugates.4,8 To synthesize PLA-pyrene conjugates, it is necessary to prepare the aldehyde-terminal PLA that can react with aminopyrene in the presence of sodium cyanoborohydride.8 To prepare the PEG-PLA-pyrene conjugate, pyrene-1-carbonyl cyanide was conjugated to the ω-hydroxyl group of the PLA end of the PEG-PLA copolymer, using quinuclidine as the catalyst.4 However, the use of toxic materials could be a critical issue in the synthesis of biomaterials. Instead, we introduced a simpler labeling method using the carboxyl group of 1-pyrenebutyric acid coupled with the hydroxyl group of PEL-PLA in the presence of DIC/HOAt. The latter is the coupling agent commonly used in peptide synthesis.
The thermal properties of PEG-PLA-pyrene were investigated using DSC and TGA and were compared with the corresponding PEG-PLA and carboxyl pyrene. For DSC measurements, samples were first heated from room temperature to 105°C and then cooled to 30°C, followed by a second heating to 220°C at a heating rate of 10°C·min−1. DSC thermograms of carboxyl pyrene, PEG-PLA, and PEG-PLA-pyrene are shown in Figure 3A. PEG-PLA-pyrene appeared semicrystalline with two melting peaks. The melting enthalpy (ΔHm) of PEG-PLA-pyrene was found to be 100 J·g−1 in the first peak and 9 J·g−1 in the second peak. PEG-PLA showed a melting temperature (Tm) value close to that of the first peak of PEG-PLA-pyrene. This finding showed that the presence of pyrene at the end of PLA did not influence the crystallization ability of the PEG blocks. However, the presence of PEG-PLA blocks strongly reduced the ΔHm and Tm of pyrene, indicating that the thermal characteristics were sensitive to PEG-PLA incorporation. TGA thermograms of the samples were registered from 30°C to 500°C at a heating rate of 10°C·min−1, as shown in Figure 3B. Pyrene and the PEG-PLA copolymer exhibited a uniform thermal degradation behavior. In the case of the PEG-PLA-pyrene copolymer, a two-step degradation was detected. It is assumed that the first degradation step was due to the pyrene moiety. The value of decomposition temperature (Td) was read with respect to a 5% weight loss of the sample; thus, a Td value of 290°C was obtained for carboxyl pyrene, and 240°C and 190°C for the copolymers PEG-PLA and PEG-PLA-pyrene, respectively. The TGA curve of PEG-PLA-pyrene shifted slightly to a lower temperature compared with PEG-PLA and pyrene, ie, the overall stability decreased due to the coupling of PEG-PLA segments and pyrene. From the processing viewpoint, the coupling of the PEG-PLA copolymer with pyrene provides a wide temperature range (from 50°C to 150°C) for thermal treatments.
Figure 3 (A) DSC and (B) TGA thermograms of 1-pyrenebutyric acid (a), PEG-PLA (b), and PEG-PLA-pyrene (c).
Characterization of the fluorescent properties of polymeric micelles was performed by dissolving 2.5 mg polymer in 1 mL pure water followed by twofold serial dilutions of the sample. After sonication, we observed an abrupt enhancement in the ultraviolet absorption at 300 and 330 nm (Figure 4A), identifying an aromatic ring structure. In addition, the higher concentration of PEG-PLA-pyrene caused detection of increased absorbance intensity. Figure 3B shows the fluorescence emission spectra of serial diluted PEG-PLA-pyrene dispersions. Similar to the absorbance, as the PEG-PLA-pyrene component in the water solution increased, the intensity of the emission spectrum increased. However, no signal characteristics were detected on the absorbance and fluorescence spectra of PEG-PLA (Figure 4A and B). Due to the sensitivity of pyrene to the environmental polarity, the ratio of the two fluorescence intensities of the peak at 370 and 380 nm was plotted against the copolymer concentration.10 Figure 4C shows that the value of the fluorescence intensity ratio inverted at 1 mg·mL−1, suggesting that the formation changes from an aqueous environment to the hydrophobic core of the micelles.1,4 The results are similar to the fluorescence spectra of PEG-PLA-pyrene in water, reported in the literature.4 Amphiphilic copolymers generally present a core–shell micellar architecture with a core consisting of hydrophobic blocks and a shell composed of chains.1 DLS measurements were performed to confirm the micelle sizes. The data showed that the PEG-PLA polymeric aqueous solution possessed micelles with a unimodal distribution, with an average diameter of 9±3 nm. It appears that coupling the pyrene moiety at the end of PLA did not significantly increase the size or size distribution of the polymeric micelles (11±1 nm). It has been shown that several pathways have been verified in the internalization of exogenous antigens by dendritic cells (DCs), such as phagocytosis, and receptor-mediated endocytosis and macropinocytosis.14 The latter is used to internalize extracellular fluid and smaller solutes, such as macromolecules and, particularly, small nanoparticles (<50 nm).15 To investigate the internalization of PEG-PLA-pyrene micelles by DCs, PEG-PLA-pyrene was incubated with murine bone marrow-derived DCs (BMDCs) for 5, 10, 20, or 30 minutes (Figure S1). At 37°C, the major internalized PEG-PLA-pyrene colocalized with early endosomes (a membrane-bound compartment inside of eukaryotic cells) after a 10-minute incubation with BMDCs. However, the internalized PEG-PLA-pyrene was undetected in early endosomes until a 30-minute incubation with BMDCs at 4°C; the internalization of PEG-PLA-pyrene by BMDCs is a temperature-dependent process. Generally, the UV–vis absorbance and fluorescence emission intensities of PEG-PLA-pyrene in aqueous solution are concentration-dependent – this is a feature of great interest for the use of the conjugate as a fluorescence probe to study the in vivo distribution as well as the internalization and intracellular localization of polymeric micelles.
Pyrene-labeled biodegradable polymer PEG-PLA-pyrene was prepared by coupling carboxyl pyrene with a PEG-PLA copolymer. Physicochemical characterization showed that the copolymer preserved the properties intrinsic to PEG-PLA; in addition, PEG-PLA-pyrene forms micelles in aqueous solutions. The results show that pyrene could serve as a useful fluorescence probe for attachment onto a polymer end group, for study of the in vivo distribution as well as the internalization and intracellular localization of polymeric micelles. These results also present a new approach to the synthesis of copolymers with functional end groups.
This study was supported by the 03A1-IVPP26-014 grant from the National Health Research Institutes of Taiwan and grant NSC-102-2320-B-400-001-MY2 from the Ministry of Science and Technology of Taiwan. The authors are grateful to Dr Yu-Cheng Chou, Institute of Biotechnology and Pharmaceutical Research of NHRI, for his help with the polymer characterization and to Dr Chung-Shi Yang, Institute of Biomedical Engineering and Nanomedicine of NHRI, for his help with the light scattering analysis.
The authors report no conflicts of interest in this work.
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