pH-Sensitive and Thermosensitive Hydrogels as Stem-Cell Carriers

Apr 11, 2016 - ABSTRACT: Stem-cell therapy has the potential to regenerate damaged heart tissue after a heart attack. Injectable hydrogels may be used...
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pH and Thermal Sensitive Hydrogels as Stem Cell Carriers for Cardiac Therapy Zhenqing Li, Zhaobo Fan, Yanyi Xu, Wilson Lo, Xi Wang, Hong Niu, Xiaofei Li, Xiaoyun Xie, Mahmood Khan, and Jianjun Guan ACS Appl. Mater. Interfaces, Just Accepted Manuscript • DOI: 10.1021/acsami.6b01374 • Publication Date (Web): 11 Apr 2016 Downloaded from http://pubs.acs.org on April 13, 2016

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pH and Thermal Sensitive Hydrogels as Stem Cell Carriers for Cardiac Therapy Zhenqing Li1,†, Zhaobo Fan1,†, Yanyi Xu1,†, Wilson Lo1, Xi Wang1, Hong Niu1, Xiaofei Li1, Xiaoyun Xie2, Mahmood Khan3, Jianjun Guan 1, 4,* 1. Department of Materials Science and Engineering, The Ohio State University, Columbus, OH, 43210 2. Department of Gerontology, Tongji Hospital, Tongji University, Shanghai, China 3. Department of Emergency Medicine, Davis Heart Lung Research Institute, The Ohio State University Columbus, OH, 43210 4. Tongji Hospital, Tongji University, Shanghai, China † These authors contributed equally to this work.

* Corresponding Author: Jianjun Guan, Ph.D. Associate Professor Department of Materials Science and Engineering The Ohio State University 2041 College Road Columbus, OH 43210 Phone: 614-292-9743 Email: [email protected]

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Abstract Stem cell therapy has the potential to regenerate damaged heart tissue after heart attack. Injectable hydrogels may be used as stem cell carriers to improve cell retention in the heart tissue. However, current hydrogels are not ideal to serve as cell carriers because most of them block blood vessels after solidification. In addition, these hydrogels have a relatively slow gelation rate (typically >60 s) that do not allow them to quickly solidify upon injection so as to efficiently hold cells in the heart tissue. As a result, the hydrogels and cells are squeezed out of the tissue leading to low cell retention. To address these issues, we have developed hydrogels that can quickly solidify at the pH of infarcted heart (6-7) at 37oC, but cannot solidify at the pH of blood (7.4) at 37oC. These hydrogels are also clinically attractive because they can be injected through catheters commonly used for minimally invasive surgeries. The hydrogels were synthesized by free radical polymerization of N-isopropyl acrylamide, propylacrylic acid, hydroxyethyl methacrylate-co-oligotrimethylene carbonate and methacrylate poly(ethylene oxide) methoxy ester. Hydrogel solutions were injectable through 0.2 mm diameter catheters at pH 8.0 at 37oC, and they can quickly form solid gels under pH 6.5 at 37oC. All the hydrogels showed pH dependent degradation and mechanical properties with less mass loss and greater complex shear modulus at pH 6.5 than at pH 7.4. When cardiosphere derived cells (CDCs) were encapsulated in the hydrogels, the cells were able to survive during a 7-day culture period. The surviving cells were differentiated into cardiac cells as evidenced by the expression of cardiac markers at both the gene and protein levels, such as cardiac troponin T, myosin heavy chain alpha, calcium channel CACNA1c, cardiac troponin I, and connexin 43. Gel integrity was found to largely affect CDC cardiac differentiation. These results suggest that the developed dual-sensitive hydrogels may be promising carriers for cardiac cell therapy. Keywords: Thermo-sensitive hydrogel; pH-sensitive hydrogel; Catheter delivery; Cardiosphere derived cells; cardiac differentiation.

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1. INTRODUCTION Cardiovascular disease is the leading cause of death in the United States. Myocardial infarction is one of the major cardiovascular diseases. Currently, coronary artery bypass surgery (CABG) and percutaneous coronary intervention (PCI) are used to re-establish the blood flow to the infarcted areas. In PCI, catheter was used in balloon based angioplasty and the placement of stent. The advantage of PCI lies in its minimally invasive strategy. However, the possibility of vessel wall damage during PCI raises the high risk of thrombogenesis.1 Another drawback of PCI is its low efficacy in revascularization of infarcted areas compared to CABG.2 Delivery of anti-coagulation drugs and vascularization growth factors during PCI is a possible solution as they can suppress thrombogenesis and stimulate angiogenesis, respectively. Currently, delivery vehicles of these drugs or biomolecules include drug eluting stent,3 polymer microspheres, 4 and hydrogels. 5-6 Nevertheless, neither CABG nor PCI strategies can regenerate new cardiomyocytes to compensate the cell loss after MI. Delivery of stem cells is considered to be a promising solution. Many types of stem cells have been used in cardiac cell therapy, including mesenchymal stem cells (MSCs) ,7-8 skeleton muscle stem cells,9 embryonic stem cell derived cardiomyocytes (ESC-CM),10-11 induced pluripotent stem cells (iPSCs),12 and cardiosphere derived cells (CDCs).13-15 CDCs are derived from endocardium biopsy and have a fast proliferation rate when cultured ex vivo. They can differentiate into endothelial cells, cardiac myocytes and smooth muscle cells.13 Therefore, CDCs are considered to be one of the promising autologous adult progenitor cells for cardiac cell therapy. Direct injection of stem cells to the infarcted area results in low cell retention and poor long-term engraftment.16-18 This is mainly due to the cellular apoptosis induced by the local harsh ischemic environment and lack of cell anchorage for survival. In our previous work, thermosensitive hydrogels loaded with anti-oxidant drugs,19 angiogenic growth factors,

20-21

or oxygen release microspheres

22

were

used to address these issues. The results showed that cell survival was significantly improved under the 3

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low oxygen/low nutrient conditions or high reactive oxygen species (ROS) environment. However, gels developed in these reports cannot be directly used for catheter based PCI delivery because they are thermosensitive only and may block the catheter during the injection. Hydrogels used for catheter delivery includes polyelectrolyte pullulan,3 in situ gelling fibrin glue,6 shapedefined alginate hydrogel,23 thermosensitive triblock copolymer PEG-PLA-PEG,24 collagen gel,25 and pH sensitive hydrogels like sulfamethazine oligomer terminated PCLA-PEG-PCLA.26 The infarcted area has a lower local pH than normal cardiac tissues due to the inflammation induced by acute MI.27-28 Therefore, a hydrogel which is responsive to the pH difference is suitable for catheter based delivery. Many polymers are introduced as potential pH sensitive hydrogel candidates for biomedical applications. Natural pH sensitive hydrogels, like collagen and chitosan, are soluble at acidic pH but form gels at neutral pH.29 Synthetic polymers provide wider prospects of pH sensitivity, with pH responsive range between 3 and 10.30 Polyacrylic acid,31-32 polymethacrylic acid33 and sulfonamide based polymers34 solidify at acidic pH, while basic pH responsive polymers including poly(amino ester),35-36 poly(tertiary amine metharcylate)37-38 and poly(2-vinylpyridine)39 can form gels at basic pH. To use catheter to deliver hydrogels into infarcted hearts, the hydrogels should be acid pH responsive as the infarcted area has lower pH than that of the normal tissue. Most acid pH responsive hydrogels are based on acrylic acid and methacrylic acid that have a pH (2-4.5) far lower than that of the infarcted tissue (6-7). 27-28 Murthy et al. found that incorporation of propylacylic acid (PAA, pKa ~6.3) into hydrogels allowed pH responsive range between 6-7.40 The synthesized thermo- and pH-sensitive poly(N-isopropyl acrylamide-copropylacrylic acid-co-butylacrylate) (PNIPAAm-PAA-BA) was used as a drug carrier for basic fibroblast growth factor.41-42 However, the non-degradable nature of PNIPAAm-PAA-BA polymer may be a limitation in cell based therapy. In this work, a family of PAA based degradable, and thermal and pH sensitive hydrogels was synthesized

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by copolymerizing NIPAAm, PAA, methacrylate poly(ethylene glycol) methyl ether (MA-PEG), and biodegradable macromer 2-hydroxyethyl methacrylate-co-oligo(trimethylene carbonate) (HEMA-oTMC) (Figure 1). Hydrogel injectability, and thermal, mechanical and degradation properties were assessed under different pH. Furthermore, cardiosphere derived cells (CDCs) were encapsulated in the hydrogels, and

cell

survival

and

cardiac

differentiation

were

evaluated

by

real-time

RT-PCR

and

immunohistochemistry.

2. EXPERIMENTAL MATERIALS AND METHODS 2.1. Materials. Diethyl propylmalonate (99%), potassium hydroxide and diethylamine (99%+) were purchased from Alfa Aesar and used without further purification. Formaldehyde solution (36.5%-38.0%) was obtained from Mallinckrodt Chemicals and used as received. Concentrated sulfuric acid was purchased from Fisher and used directly. NIPAAm, MA-PEG, and 2-hydroxyethyl methacrylate (HEMA) were purchased from VWR. NIPAAm was recrystallized three times by hexane. MA-PEG and HEMA were purified by vacuum distillation. Trimethylene carbonate was obtained from Boehringer Ingelheim and used without further purification. All solvents were purchased from VWR and used as received. 2.2. Synthesis of PAA. PAA was synthesized following the methods in previous reports40, 43 with modification (Figure 2). Briefly, 50g of diethyl propylmalonate was stirred in 350 mL of 1 mol/L KOH and 95% ethanol solution overnight. The mixture was condensed by rotary evaporator. Hydrochloride acid was further added to the yellowish oil and the solution pH was adjusted to 1.5-2. 600 mL of ethyl ether was used to extract the crude product. The ether layer was further dried by magnesium sulfate overnight and filtered. Excess ether was removed by rotary evaporator. The oily product was further mixed with 27.5 mL of diethylamine at 0°C. After mixing, 21.8 mL of formaldehyde solution was slowly added by addition funnel. Following stirring for overnight, the addition funnel was replaced by a condenser. The mixture was heated up to 60°C and stirred for another 12 h. The mixture was then cooled to 0°C with addition of sulfuric acid. Ether was further used to extract the product. The structure of crude 5

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ethyl 2-propylacrylate was verified by 1H-NMR. It was further hydrolyzed by 1 mol/L KOH and reflux under 60°C. Hydrochloride acid was used to adjust pH to 1.5-2. A yellow oil-like crude product was separated and further extracted by diethyl ether. The final product was obtained by removing the ether with rotary evaporator. The structure of final PAA was verified by 1H-NMR (Figure 3): δ 6.28 (1H, s, CH2=), 5.64 (1H, s, CH2=), 2.28 (2H, t, -CH2-), 1.49 (2H, m, -CH2-) and 0.92 (3H, m, CH3-). 2.3. Synthesis of poly(NIPAAm-co-PAA-co-HEMA-oTMC-co-MA-PEG) copolymer. HEMAoTMC was synthesized based on previously reported methods.

19, 43

The obtained HEMA-oTMC had an

average of 2.2 TMC units calculated from the 1H-NMR spectrum. The copolymer poly(NIPAAm-coPAA-co-HEMA-oTMC-co-MA-PEG) was synthesized via free radical polymerization of NIPAAm, PAA, HEMA-oTMC and MA-PEG (Figure 4). The monomers and macromer were dissolved in dioxane and charged in a 250 mL round bottom flask. Benzoyl peroxide was used as initiator. The reaction was conducted at 60°C for overnight under the protection of nitrogen. The polymer was precipitated by hexane, purified by tetrahydrofuran/ethyl ether twice and dried under vacuum. 2.4. Characterization of synthesized hydrogels. Structure of the copolymers was characterized by 1

H-NMR. The composition was determined by the ratio between the integration of characteristic peaks of

different functional groups. The molecular weight and polydispersity index (PDI) of the copolymers were determined by gel permeation chromatography (GPC). THF and polystyrene were used as the solvent and standards, respectively. The hydrogel solutions were prepared by dissolving copolymers in Dubecco's modified phosphate buffer saline (DPBS). The final concentration was 20 wt%. The injectability of the hydrogel solutions was tested by injecting the pre-warmed solutions (37oC) through a catheter (Abbott Voyage, inner diameter 0.2 mm) to 37oC sodium phosphate buffers with pH of 6.5 and 7.4, respectively. The catheter was immersed in a 37oC water bath. The lower critical solution temperatures (LCSTs) of the solutions at pH of 6.5, 7.4 and 8.0 were measured by DSC using a thermal scanning from 0°C to 60°C with a 10°C/min increment. The temperature at the maximum endothermal peak was considered as LCST. 6

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Solid gels were formed by incubating the hydrogel solutions in pH 6.5 buffer at 37°C. To determine the pH responsiveness, hydrogels were equilibrated under sodium phosphate buffer of either pH 6.5 or 7.4 for 24 h. The rationale of using sodium phosphate buffer was to test gel response under different pH without changing ionic strength. For mechanical test, hydrogels were placed into a cone-plate rheometer equipped with temperature controlled Peltier and a cap to prevent evaporation. Gap distance was set to be the thickness of gels. A strain sweep (0.1% to 3%) with a 1 Hz frequency was used. A further frequency sweep from 1 Hz to 10 Hz with strain in linear viscoelastic region was applied. The storage, loss modulus and the complex viscosity was recorded. Afterwards, a large strain sweep from 0.1% to 15% was further used. Hydrogel water content was determined based on the wet weight of the hydrogel w1, and the lyophilized weight w2. The water content was calculated as: water content (%) = (w1-w2)/w2 × 100% Hydrogel degradation was conducted in pH 6.5 and 7.4 buffers respectively to investigate the effect of pH on degradation rate. The solid hydrogels were placed in 2 ml microcentrifuge tubes containing 1.5 ml of pre-warmed buffer. The degradation was conducted in a 37°C water bath. The samples were taken at defined intervals and freeze-dried before being weighed (w3). The weight loss was calculated as:

Weight remaining (%) = w3/w4 × 100 %

where w4 is the sample weight before degradation.

2.5. Encapsulation of cardiosphere derived cells (CDCs) into hydrogels. Murine CDCs were cultured by using Iscove modified Dubecco's medium (IMDM) supplemented with 10% fetal bovine

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serum, 2% L-glutamine and 1% antibiotics. The medium was changed every three days. Cells were passaged when 90% confluence was reached. CDCs of passages 11-14 were used. CDC suspension with density of 20 million/mL was prepared by trypsinizing and resuspending cells in DPBS. 0.5 mL of cell suspension was added into 1 mL of hydrogel solution at 4°C and mixed thoroughly. Hydrogel/cell constructs were then formed by incubating the mixture at 37°C for 20-30 min. Supernatant was replaced by equal amount of cell culture medium (pH 7.4). 2.6. Survival and cardiac differentiation of CDCs in hydrogels. To assess cell survival, cell/hydrogel constructs were collected after 1 and 7 days of culture followed by digestion in papain solution at 60°C. The double stranded DNA (dsDNA) content in the solution was quantified by PicoGreen assay (Invitrogen). To assess cardiac differentiation of the encapsulated CDCs at the gene level, cell/hydrogel constructs were first immersed into TRIzol (Sigma) to isolate total RNA following manufacturer’s protocol. The quality of RNA was monitored by Nanodrop system. Total of 1 µg RNA was utilized to synthesize cDNA. Primers of forward and reverse pairs of cardiac troponin T (cTnT), myosin heavy chain alpha (MYH6) and calcium channel, voltage-dependent, L type, alpha 1c (CACNA1c), and β-actin were designed using PerlPrimer software. The sequences and melting temperatures are listed in Table 1. Real-time RT-PCR was conducted in triplicate for each sample with Maxima SYBR Green/fluorescein master mix on an Applied Biosystem 7900 system. β-Actin was used as the housekeeping gene. Fold differences were calculated using standard ∆∆Ct method. To assess CDC cardiac differentiation at the protein level, cell/hydrogel constructs were taken after 7 days of culture, and fixed in 4% paraformaldehyde for 1 h. The constructs were further embedded in optimal cutting temperature (OCT) solution and sectioned at -20°C with a thickness of 10 µm. The sections were blocked by 10% goat serum, permeabilized by 0.3% Triton X-100 for 1 h, incubated with primary antibodies mouse anti-mouse cTnI (Abcam) and rabbit anti-mouse connexin 43 at 37°C overnight, and finally incubated with secondary antibodies Dylight488 conjugated goat anti-mouse IgG and 8

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AlexaFluo647 conjugated goat anti rabbit IgG (Jackson Immuno) at 37°C for 1 h. Hoechst 33342 was used to counter-stain the nucleus. Sections without primary antibody incubation were treated as negative control. All images were observed under Olympus FV1000 confocal microscope. 2.7. Statistical analysis. Data are reported as mean ± standard deviation. Multivariate repeatedmeasures ANOVA were used to compute statistical significance between different groups. A statistical significance was considered when p