明胶
自愈水凝胶
顺铂
体内
体外
化学
药理学
生物医学工程
生物化学
医学
高分子化学
化疗
外科
生物
生物技术
作者
Takahisa Suzuki,Shigeru Tsunoda,Kota Yamashita,Toshie Kuwahara,Mitsuru Ando,Yasuhiko Tabata,Kazutaka Obama
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-11-25
卷期号:14 (12): 2601-2601
标识
DOI:10.3390/pharmaceutics14122601
摘要
The objective of this study was to develop a new preparation method for cisplatin (CDDP)-incorporated gelatin hydrogels without using chemical crosslinking nor a vacuum heating instrument for dehydrothermal crosslinking. By simply mixing CDDP and gelatin, CDDP-crosslinked gelatin hydrogels (CCGH) were prepared. CDDP functions as a crosslinking agent of gelatin to form the gelatin hydrogel. Simultaneously, CDDP is incorporated into the gelatin hydrogel as a controlled release carrier. CDDP’s in vitro and in vivo anticancer efficacy after incorporation into CCGH was evaluated. In the in vitro system, the CDDP was released gradually due to CCGH degradation with an initial burst release of approximately 16%. CDDP metal-coordinated with the degraded fragment of gelatin was released from CCGH with maintaining the anticancer activity. After intraperitoneal administration of CCGH, CDDP was detected in the blood circulation while its toxicity was low. Following intraperitoneal administration of CCGH in a murine peritoneal dissemination model of human gastric cancer MKN45-Luc cell line, the survival time was significantly prolonged compared with free CDDP solution. It is concluded that CCGH prepared by the CDDP-based crosslinking of gelatin is an excellent sustained release system of CDDP to achieve superior anticancer effects with minimal side effects compared with free CDDP solution.
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