Sustained release of VEGF from PLGA nanoparticles embedded thermo-sensitive hydrogel in full-thickness porcine bladder acellular matrix
© Geng et al; licensee Springer. 2011
Received: 20 December 2010
Accepted: 7 April 2011
Published: 7 April 2011
We fabricated a novel vascular endothelial growth factor (VEGF)-loaded poly(lactic-co-glycolic acid) (PLGA)-nanoparticles (NPs)-embedded thermo-sensitive hydrogel in porcine bladder acellular matrix allograft (BAMA) system, which is designed for achieving a sustained release of VEGF protein, and embedding the protein carrier into the BAMA. We identified and optimized various formulations and process parameters to get the preferred particle size, entrapment, and polydispersibility of the VEGF-NPs, and incorporated the VEGF-NPs into the (poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (Pluronic®) F127 to achieve the preferred VEGF-NPs thermo-sensitive gel system. Then the thermal behavior of the system was proven by in vitro and in vivo study, and the kinetic-sustained release profile of the system embedded in porcine bladder acellular matrix was investigated. Results indicated that the bioactivity of the encapsulated VEGF released from the NPs was reserved, and the VEGF-NPs thermo-sensitive gel system can achieve sol-gel transmission successfully at appropriate temperature. Furthermore, the system can create a satisfactory tissue-compatible environment and an effective VEGF-sustained release approach. In conclusion, a novel VEGF-loaded PLGA NPs-embedded thermo-sensitive hydrogel in porcine BAMA system is successfully prepared, to provide a promising way for deficient bladder reconstruction therapy.
A variety of congenital and acquired conditions cause compromised bladder capacity and compliance. The major surgical solution is enterocystoplasty, whereby the functionally deficient bladder is reconstructed using biomaterials. In terms of biomaterials for bladder reconstruction, bladder acellular matrix allograft (BAMA) [1, 2] has great potential for complete and functional regeneration of the bladder. BAMA is a naturally derived biodegradable material that is currently being developed for use as a bladder substitute. It is produced by extracting the cells and soluble matrix components from the extracellular matrix, and so it has almost all the properties of a normal bladder, and maintains a low potential for inflammatory attack on the graft because most of the antigenic proteins are extracted from the bladder tissue. The long-term follow-up of vascular acellular matrix allografts has demonstrated their biocompatibility [3–5].
Previous research has proven that the administration of growth factors can promote tissue revascularization. Under an appropriate dosage, pro-angiogenic cytokines, such as vascular endothelial growth factor (VEGF) [6, 7], can up-regulate angiogenesis by signaling vascular endothelial cells to undergo proliferation, migration, and differentiation into new blood vessels. However, the short-lived effect and high instability (such as oxidation, deamidation, and diketopiperazine formation in a physiological environment) of the VEGF protein result in some disappointing clinical trials, because the therapeutic effects of the protein can only be achieved at extremely high doses, which often results in side effects such as the progression of malignant vascular tumors . A superior formulation is needed to deliver VEGF continuously to maintain the VEGF concentration within the therapeutic window during the long term of tissues' reconstruction.
In this study, we report a novel VEGF-loaded nanoparticles (NPs)-embedded porcine bladder acellular matrix with thermo-response system, which is designed for achieving a sustained release of VEGF protein, and embedding the protein carrier into the BAMA. For the incorporation and sustained release of VEGF, the protein was encapsulated in NPs with biodegradable poly(lactic-co-glycolic acid) (PLGA) by multi-emulsion and solvent evaporation methods, which result in the protein-loaded round-shaped NPs [9, 10]. Then, the VEGF-loaded PLGA NPs are combined with a hydrophilic gel matrix, (poly(ethylene oxide)-poly(propylene oxide)-poly(ethylene oxide) (Pluronic®) F127 hydrogel , using the sol-gel transition to give a well-dispersed PLGA particles-embedded hydrogel . Finally, the VEGF-NPs-F127 gel was embedded in BAMA with multipoint injection. Such a strategy as this allows the carrier system to show a sustained release of protein, a retention of protein-loaded NPs in BAMA, as well as additional properties such as thermo-sensitivity and biocompatibility.
Pluronic® F127 triblock copolymer, Tween® 80 (polyoxyethylene sorbitan monooleate), and poly(vinyl alcohol) (PVA) (Mw 14-16 kDa) were purchased from Sigma-Aldrich (Shanghai, China). PLGA with a monomer ratio (lactic acid/glycolic acid) of 50:50 was purchased from Daigang Biomaterial Co., Ltd. (Jinan, China). rhVEGF165 and rhVEGF enzyme-linked immunosorbent assay (ELISA) kit was purchased from Peprotech (Rocky Hill, NJ, USA), and all other reagents were purchased from Sigma-Aldrich.
Preparation of NPs-embedded thermo-sensitive hydrogel
PLGA NPs containing VEGF (0.1 μg/mg of NPs) were prepared by the double emulsion-solvent evaporation technique based on the method of Liao et al. . In briefly, 20 mg of PLGA was dissolved in appropriate amount of dichloromethane. This polymer solution was injected into 100 μL of phosphate-buffered saline, pH7.4 (PBS7.4) as the inner aqueous phase (W1) containing VEGF, heparin (Hp, 16 kDa), and human serum albumin (HSA) (VEGF/Hp/HSA 1:1:500, w/w/w). Next, the previously formed inner emulsion (W1/O) was generated by a high-speed homogenizer of IKA ultra turrax operating at 3,000 rpm for 2 min. Then, the first emulsion was injected into 10 mL outer aqueous phase (W2), which was composed of aqueous 1.5% (w/v) PVA and 2% Tween80, resulting in a multiple emulsion (W1/O/W2), which was homogenized by ultra turrax at specific speed and time following an incubation on ice. This emulsion was put on a rota-evaporator under vacuum (500 mHg) for 3 h at room temperature for complete solvent evaporation. The organic phase was evaporated leading to precipitation of polymer to get the NPs, which hardens over time. The NPs were collected by centrifugation at 10,000 × g for 5 min at 4°C and washed with distilled water three times followed by freeze-drying using mannitol as cryoprotectant (PLGA:Mannitol:100:30) to get dry powder containing NPs.
Experimental design matrix with observed values of the objectives variables of protein-loaded NPs
E.E.(%) ± SD (n= 6)
35.29 ± 0.07
38.82 ± 0.53
51.76 ± 0.28
50.59 ± 0.46
48.82 ± 0.12
54.71 ± 0.09
42.94 ± 0.14
55.88 ± 0.10
44.12 ± 0.74
45.88 ± 0.67
50.00 ± 0.41
52.35 ± 0.75
44.71 ± 0.69
49.41 ± 0.21
47.06 ± 0.55
Fluorescent probes-loaded NPs were obtained by adding hydrophilic CdTe quantum dots (QDs) (1 μg/mg of NPs, prepared according to our previous report with maximum emission wavelength of 590 nm)  into the inner aqueous phase instead of VEGF protein, and the NPs prepared as described produced optimized results. The NPs containing only Hp and HSA were produced as negative control.
Then, the accurate NPs (lyophilized) were resuspended in distilled water. This suspension was added to the concentrated F127 solution so that the final F127 concentration reached 25% w/v and stirred gently for 10 min after incubation on ice for uniform distribution of NPs in the F127 solution.
NPs morphology and particle size
The formulations prepared by double emulsification solvent evaporation were performed for shape and surface morphology using a Zeiss Ultra 55 scanning electron microscope (SEM). The dried NP samples were suspended in distilled water until further examination.
Particle diameter was determined using a Nicomp 380ZLS particle sizing system. Accordingly, the dried NP samples were suspended in distilled water. The obtained homogenous suspensions were examined to determine the mean diameter and polydispersity index.
Determination of encapsulation efficiency
The NP encapsulation efficiency (E.E.) was determined upon their separation from the aqueous preparation medium containing the non-associated protein by centrifugation (20,000 × g, 4°C, 10 min). The amount of free protein was determined in the supernatant using a bicinchoninic acid assay. The extraction procedure was performed for a total of 3 × for each particle type. The NP E.E. was calculated using the following equation: E.E. (%) = [(Total protein amount - Free protein amount)/Total protein amount] × 100%.
Gelation temperature and thermo-reversible behavior in vivo
The gelation temperatures of varying concentration (w/v) of Pluronic F127 were determined by the tube inversion method. In brief, accurate F127 was dissolved in ultrapure water at cold temperature in Eppendorf tube, the tubes were reversed constantly and the temperature at which the solution stopped dropping was measured; at this temperature, the solution was converted into gel. The thermo-reversibility was verified by giving repeated cooling and heating cycles to confirm any change in the gelation temperature and reversibility of gel-sol behavior.
To confirm the thermo-sensitive, sustained release properties of the NPs-embedded hydrogel, physiologically normal nude mice were treated with QDs-NPs-F127 gel, QDs-NPs, and QDs-physiological saline solution, and they were all treated with aliquots QDs dosage of 2 mg/kg via subcutaneous injection. In vivo mouse images were acquired using a Berthold Night OWL in vivo imager. Fluorescence images of all the experimental mice were taken continuously for 24 h along with the typical images at 10 min post-injection.
In vitro drug release of VEGF-loaded NPs-embedded thermo-sensitive hydrogel was evaluated in buffer solution. In brief, 10 mg of dried NPs was suspended in 0.2 mL 25% Pluronic® F127 solution, and then the solution was rapidly pushed into a 2 cm2 full-thickness porcine bladder acellular matrix through multipoint sequential injection. The matrix was dipped into 2 mL phosphate buffer saline (PBS) at pH 7.4 and at 37°C, which had previously been filtered on 0.22-μm sterile filters and microbiologically preserved with 0.02%w/w sodium azide. Then, the release media were placed in a thermostatic bath at 37°C. At scheduled time intervals, the release medium was withdrawn and replaced with the equal volume of fresh, filtered medium. Release of VEGF from NPs, 25% Pluronic® F127, and NPs-embedded 25% Pluronic® F127 were tested at the same time as references. Samples were centrifuged (20,000 × g, 4°C, 10 min), and the supernatant was analyzed for VEGF content via ELISA using the VEGF ELISA kit as per the manufacturer's protocol. Results are expressed as cumulative release of VEGF NPs ± SD (standard deviation) of three replicates.
Bioactivity of released VEGF
The bioactivity of the VEGF released from the microparticles was evaluated in vitro by determining the proliferative capacity of an endothelial cell line (human umbilical vein endothelial cell, HUVEC) after VEGF treatment. First, VEGF-loaded NPs were incubated in Endothelial Cell Growth Medium-2 (EGM-2) without growth factors for a continuous period of 1, 5, 10, or 15 days, the release EGM-2 medium was filtered with 0.22-μm sterile filters and VEGF values were measured using ELISA and stored at 4°C. Second, HUVEC were cultured in EGM-2 media supplemented with 30 μg/mL endothelial cell growth supplement, 10% fetal bovine serum, 1% Hp, and 1% penicillin/streptomycin. In order to determine the endothelial cell proliferation capacity after VEGF stimulation, the HUVEC were placed into 96-well culture plates with a density of 1 × 103cells/well and allowed to adhere overnight. Medium was then aspirated, and the released EGM-2 medium supernatant from VEGF-loaded NPs was then added to wells immediately to make an equivalent final VEGF concentration of 10 or 20 ng/mL. Native, non-encapsulated VEGF at 10 or 20 ng/mL was used as the 100% bioactivity benchmark, and wells with medium only (no VEGF), as well as the released EGM-2 medium supernatant from non-loaded NPs, were employed as the negative control. Cells were incubated for 3 days, and the number of viable cells in each experimental group was determined by the 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay.
Data presentation and statistical analyses
Unless otherwise indicated, data are represented as mean ± SD. Statistical significance was determined using a student's t-test with a 95% confidence interval, unless otherwise noted. Statistical calculations were performed using a SPSS software.
Results and discussion
Preparation of NPs is a complex procedure as it involves several processing variables and design components [15, 16]. Even slight changes of these variables and system components can have significant impact on the quality of final product. Unique attributes of NPs such as particle size and entrapment efficiency are of utmost importance from the biological and pharmaceutical point of view [17–19]. Particles with smaller average diameter showed slower release. Smaller particles are generally formed with higher impact . It varies the tortuous polymeric diffusion pathways in smaller particles . This ultimately leads to a sustained diffusion of protein from the particles. Another quality attribute of NPs is the entrapment efficiency which should be properly optimized to avoid the loss of drug during processing . It is of the highest importance especially in case of drugs such as VEGF, with their cost being very high. Here, we choose the particle diameter and the entrapment efficiency as the experimental investigation response. Using the double emulsion method for preparation of NPs, the second emulsification is decisive for the size of the NPs. Thus, the intensity and the time of emulsification can be used for controlling size. Here, we selected three critical factors, namely, volume ratio of organic solvent phase to external aqueous phase, agitation speed, and duration of homogenization for the optimization of the experimental investigation response.
Table 1 depicts the various process parameters of the prepared protein containing NPs. The results of the particle size analysis by laser diffraction showed that particle sizes varied from 280.8 to 2503.5 nm with variable polydispersity indices among the experimental formulations. Among them, formulation 1 had the least value of the average diameter, whereas 12 had the maximum. The polydispersibility indices also showed the similar patterns of dispersibilities, i.e., formulation 2 had the least value and 6 had the maximum. The data suggest that with increasing homogenizing speed, average diameters of particles were reduced. However, when speed of homogenization was further enhanced, the protein E.E. reduced too, Therefore, after all these results having been considered, experiment 5 was concluded to be the optimized one for the preparation of the protein-loaded NPs.
A thermo-sensitive hydrogel-entrapped VEGF-NPs system has been prepared and characterized in this study. Various formulations and process parameters were identified and optimized to obtain the preferred particle size, entrapment, and polydispersibility of the VEGF-NPs system. Then, the thermo-sensitive behavior was proven by the in vitro and in vivo study, and the kinetic sustained release profile of the VEGF-NPs-F127 gel system embedded in porcine bladder acellular matrix was investigated. Results indicate that the thermal responsive VEGF-NPs-F127 gel system prevents acute tissue reaction, inflammation, and toxic manifestation because the gel creates a tissue-compatible environment and an effective VEGF sustained release approach. The proposed system provides a promising way for deficient bladder reconstruction therapy. Entrapment of growth factor drugs into this kind of nanohydrogels for deficient bladder reconstruction therapy will form the scope of our future study.
bladder acellular matrix allograft
enzyme-linked immunosorbent assay
human serum albumin
human umbilical vein endothelial cell
scanning electron microscope
phosphate buffer saline
vascular endothelial growth factor.
This study is supported by Shanghai Committee of Science and Technology (8411964700), the National Natural Scientific Fund (30973135), the National 973 Project (2010CB933901 and 2011CB933100), the National 863 Hi-tech Project (2007AA022004), Important National Science & Technology Specific Projects (2009ZX10004-311), Special Project for Nanotechnology from Shanghai (1052nm04100), New Century Excellent Talent of Ministry of Education of China (NCET-08-0350), and Shanghai Science and Technology Fund (10XD1406100). The authors appreciate the support received from the Instrumental Analysis Center of Shanghai Jiao Tong University during the characterization of materials.
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