Sarwar Muhammad Sohail, Huang Qingrong, Ghaffar Abdul, Abid Muhmmad Amin, Zafar Muhammad Sohail, Khurshid Zohaib, Latif Muhammad
Department of Chemistry, University of Engineering and Technology, Lahore 54890, Pakistan.
Department of Food Science, Rutgers, The State University of New Jersey, New Brunswick, NJ 08901, USA.
Pharmaceutics. 2020 Feb 4;12(2):131. doi: 10.3390/pharmaceutics12020131.
The amalgamation of natural polysaccharides with synthetic polymers often produces fruitful results in the area of drug delivery due to their biodegradable and biocompatible nature. In this study, a series of blend films composed of chitosan (CS)/poly(allylamine hydrochloride) (PAH) in different compositions were prepared as smart drug delivery matrices. The properties of these polymeric films were then explored. Attenuated total reflectance-Fourier transform infrared (ATR-FTIR) analysis confirmed an intermolecular hydrogen bonding between CS and PAH. Atomic force microscopy (AFM) revealed improvements in surface morphology as the percentage of PAH in the blend films increased up to 60% (w/w). Water contact angle (WCA) ranged between 97° to 115°, exhibiting the hydrophobic nature of the films. Two films were selected, CTH-1 (90% CS and 10% PAH) and CTH-2 (80% CS and 20% PAH), to test for in vitro cumulative drug release (%) at 37 ± 0.5 °C as a function of time. It was revealed that for simulated gastric fluid (SGF) with pH 1.2, the cumulative drug release (CDR) for CTH-1 and CTH-2 was around 88% and 85% in 50 min, respectively. Both films converted into gel-like material after 30 min. On the other hand, in pH 7.4 phosphate buffer saline (PBS) solution, the maximum CDR for CTH-1 and CTH-2 was 93% in 90 min and 98% in 120 min, respectively. After 120 min, these films became fragments. Sustained drug release was observed in PBS, as compared to SGF, because of the poor stability of the films in the latter. These results demonstrate the excellent potential of blend films in sustained-release drug delivery systems for hydrophilic or unstable drugs.
由于天然多糖具有可生物降解和生物相容性的特性,其与合成聚合物的融合在药物递送领域常常能产生丰硕的成果。在本研究中,制备了一系列不同组成的壳聚糖(CS)/聚(烯丙胺盐酸盐)(PAH)共混膜作为智能药物递送基质。然后对这些聚合物膜的性能进行了探究。衰减全反射傅里叶变换红外光谱(ATR-FTIR)分析证实了CS和PAH之间存在分子间氢键。原子力显微镜(AFM)显示,随着共混膜中PAH的百分比增加至60%(w/w),表面形态得到改善。水接触角(WCA)在97°至115°之间,表明膜具有疏水性。选择了两种膜,CTH-1(90% CS和10% PAH)和CTH-2(80% CS和20% PAH),在37 ± 0.5 °C下测试其作为时间函数的体外累积药物释放率(%)。结果表明,对于pH值为1.2的模拟胃液(SGF),CTH-1和CTH-2在50分钟内的累积药物释放率(CDR)分别约为88%和85%。两种膜在30分钟后都转变为凝胶状物质。另一方面,在pH值为7.4的磷酸盐缓冲盐水(PBS)溶液中,CTH-1和CTH-2的最大CDR分别在90分钟内为93%和在120分钟内为98%。120分钟后,这些膜变成了碎片。与SGF相比,在PBS中观察到了药物的持续释放,这是因为膜在后者中的稳定性较差。这些结果证明了共混膜在亲水性或不稳定药物的缓释药物递送系统中具有优异的潜力。