Han Haijie, Li Su, Zhong Yueyang, Huang Yue, Wang Kai, Jin Qiao, Ji Jian, Yao Ke
Eye Center, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
Zhejiang Provincial Key Lab of Ophthalmology, the Second Affiliated Hospital, School of Medicine, Zhejiang University, Hangzhou 310009, China.
Asian J Pharm Sci. 2022 Jan;17(1):35-52. doi: 10.1016/j.ajps.2021.06.001. Epub 2021 Jul 1.
Gemcitabine has been extensively applied in treating various solid tumors. Nonetheless, the clinical performance of gemcitabine is severely restricted by its unsatisfactory pharmacokinetic parameters and easy deactivation mainly because of its rapid deamination, deficiencies in deoxycytidine kinase (DCK), and alterations in nucleoside transporter. On this account, repeated injections with a high concentration of gemcitabine are adopted, leading to severe systemic toxicity to healthy cells. Accordingly, it is highly crucial to fabricate efficient gemcitabine delivery systems to obtain improved therapeutic efficacy of gemcitabine. A large number of gemcitabine pro-drugs were synthesized by chemical modification of gemcitabine to improve its biostability and bioavailability. Besides, gemcitabine-loaded nano-drugs were prepared to improve the delivery efficiency. In this review article, we introduced different strategies for improving the therapeutic performance of gemcitabine by the fabrication of pro-drugs and nano-drugs. We hope this review will provide new insight into the rational design of gemcitabine-based delivery strategies for enhanced cancer therapy.
吉西他滨已被广泛应用于治疗各种实体瘤。然而,吉西他滨的临床性能受到其不理想的药代动力学参数和易失活的严重限制,主要原因是其快速脱氨、脱氧胞苷激酶(DCK)缺乏以及核苷转运体的改变。因此,采用高浓度吉西他滨重复注射,对健康细胞产生严重的全身毒性。因此,构建高效的吉西他滨递送系统以提高吉西他滨的治疗效果至关重要。通过对吉西他滨进行化学修饰合成了大量吉西他滨前药,以提高其生物稳定性和生物利用度。此外,还制备了载有吉西他滨的纳米药物以提高递送效率。在这篇综述文章中,我们介绍了通过制备前药和纳米药物来提高吉西他滨治疗性能的不同策略。我们希望这篇综述能为基于吉西他滨的递送策略的合理设计提供新的见解,以增强癌症治疗效果。