Controlled drug release contenders comprising starch/poly(allylamine hydrochloride) biodegradable composite films

被引:3
|
作者
Sarwar, Muhammad Sohail [1 ,2 ,3 ]
Ghaffar, Abdul [1 ]
Huang, Qingrong [2 ]
Khalid, Meraj [4 ]
Anwar, Aneela [5 ]
Alayoubi, Abdulfatah M. [6 ]
Latif, Muhammad [6 ,7 ]
机构
[1] Univ Engn & Technol, Dept Chem, Lahore 54890, Pakistan
[2] State Univ New Jersey, Dept Food Sci, Rutgers, New Brunswick, NJ 08901 USA
[3] Chartered Univ, Forman Christian Coll, Dept Chem, Lahore 54600, Pakistan
[4] Nishtar Med Univ, Multan 66000, Pakistan
[5] Univ Engn &Technol, Dept Basic Sci & Humanities, KSK Campus, Lahore 54000, Pakistan
[6] Taibah Univ, Coll Med, Dept Biochem & Mol Med, Madinah 42318, Saudi Arabia
[7] Taibah Univ, Ctr Genet & Inherited Dis CGID, Madinah 42318, Saudi Arabia
关键词
Biomaterials; Metabolic diseases; Drug release; Simulated gastric fluid; Phosphate buffer saline; Tissue engineering; CHITOSAN; DELIVERY; NANOPARTICLES; BLENDS; POLYALLYLAMINE; FORMULATION; SODIUM; CIPROFLOXACIN; FABRICATION; HYDROGEL;
D O I
10.1016/j.ijbiomac.2023.124598
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The blending of natural polysaccharides with synthetic polymers has attracted much attention in drug delivery models owing to their remarkable biodegradable and biocompatible characteristics. This study focuses on the facile preparation of a sequence of composite films having Starch/Poly(allylamine hydrochloride) (ST/PAH) in different compositions to propose a novel drug delivery system (DDS). ST/PAH blend films were developed and characterized. FT-IR evaluation confirmed the involvement of intermolecular H-bonding between the ST and PAH counterparts in blended films. The water contact angle (WCA) ranged from 71 degrees to 100 degrees indicating that all the films were hydrophobic. TPH-1 (90 % ST and 10 % PAH) was evaluated for in vitro controlled drug release (CDR) at 37 +/- 0.5 degrees C in a time-dependent fashion. CDR was recorded in phosphate buffer saline (PBS) and simulated gastric fluid (SGF). In the case of SGF (pH 1.2), the percentile drug release (DR) for TPH-1 was approximately 91 % in 110 min, while the maximum DR was 95 % in 80 min in PBS (pH 7.4) solution. Our results demonstrate that the fabricated biocompatible blend films can be a promising candidate for a sustained-release DDS for oral drug administration, tissue engineering, wound dressings, and other biomedical applications.
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页数:9
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