Small intestine- and colon-specific smart oral drug delivery system with controlled release characteristic
- Authors
- Kang, Ji-Hye; Hwang, Ji-Young; Seo, Jae-Won; Kim, Han-Sem; Shin, Ueon Sang
- Issue Date
- 1-10월-2018
- Publisher
- ELSEVIER SCIENCE BV
- Keywords
- pH- and temperature-responsive copolymer; Oral drug-delivery systems; Small intestine; Colon; Controlled delivery
- Citation
- MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS, v.91, pp.247 - 254
- Indexed
- SCIE
SCOPUS
- Journal Title
- MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS
- Volume
- 91
- Start Page
- 247
- End Page
- 254
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/72523
- DOI
- 10.1016/j.msec.2018.05.052
- ISSN
- 0928-4931
- Abstract
- In recent years, there has been a significant increase in strategies for the development of small intestine (and colon)-specific oral drug-delivery systems to maximize the efficiency of therapeutic agents and reduce side effects. However, only a few strategies are capable of working in the complicated environment of the human intestinal tract. In this study, the preparation of a basic pH/temperature-responsive co-polymer (p-NIVIm) and its its-vitro-drug delivery function in the pH range of 1-8 and temperature range of 25-42 degrees C are reported. The basic copolymer was prepared by radical copolymerization of N-isopropyl acryl amide (NIPAAm) and N-vinylimidazole (VIm). The lower critical solution temperature (LCST) of p-NIVIm was higher in stomach pH (similar to 1.0) conditions (36.5-42 degrees C) and lower in small intestine and/or colon pH (similar to 8.0) conditions (35.8-38.2 degrees C). The ability to uptake a model protein (BSA) at body temperature and to release it in conditions of 37 degrees C and pH 1-8 was determined. The drug loading capacity (0.231 mg per 1.0 mg copolymer) and efficiency (92.4%) were high at 37 degrees C/pH 7. The drug carrier showed a slow release pattern at pH 1 (similar to 0.084 mg; similar to 35%) and then a sudden release pattern (similar to 0.177 mg; similar to 73%) at pH 8. The cytotoxicity of p-NIVIm to MCF-7 cells in vitro was minimal at concentrations < 168.9 mu g/mL after 72 h. The prepared copolymer with its pH-/temperature-responsive protein-entrapping and -releasing behavior at body temperature may potentially be applied as a novel small intestine (and colon)-specific oral drug delivery system.
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