Wang Yaowen, Ma Jingjing, Qiu Tong, Tang Mingxiu, Zhang Xueqiong, Dong Weiguo
Department of Pharmaceutical Engineering, School of Chemistry, Chemical Engineering and Life Sciences, Wuhan University of Technology, Wuhan 430070, China.
Department of Gastroenterology, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, 430070, China; Department of Geriatrics, Renmin Hospital of Wuhan University, Wuhan, Hubei Province, Wuhan 430060, China.
Eur J Pharm Sci. 2021 Aug 1;163:105864. doi: 10.1016/j.ejps.2021.105864. Epub 2021 May 6.
Oxaliplatin (OXE) combined with other chemotherapy drugs against colorectal cancer had been reported in the literature before, however, the efficacy of oxaliplatin combined with natural compounds was elusive. In addition, the clinical bioactivity and therapeutic dose of antitumor drugs are severely limited due to poor targeting and side effects. NDDSs offers an excellent strategy to overcome the disadvantages of small molecule anticancer drugs.
Here, we have prepared N,O-carboxymethyl chitosan Oxaliplatin nanoparticles (CMCS-OXE NPs) and N,O-carboxymethyl chitosan Resveratrol nanoparticles (CMCS-Res NPs) were prepared by ion crosslinking and emulsification crosslinking, respectively.
The results revealed that the CMCS-OXE NPs exhibited a high encapsulation efficiency (60%) with a size of approximately 190.0 nm, and the CMCS-Res NPs exhibited a high encapsulation efficiency (65%) with a size of approximately 164.2 nm. The treatment with both types of nanoparticles combined exhibited more significant anti-colon cancer activity than the free drugs or either type of nanoparticle alone. In the in vivo experiments, the inhibition efficiency of the combined nanoparticle treatment was much stronger than the free drugs or either type of nanoparticle alone.
Overall, combination of oxaliplatin and resveratrol into a nanoparticle-drug delivery systems (NDDSs) appears to be a promising strategy for colorectal cancer (CRC) therapy.
此前文献中已有奥沙利铂(OXE)与其他化疗药物联合用于治疗结直肠癌的报道,然而,奥沙利铂与天然化合物联合使用的疗效尚不明确。此外,由于靶向性差和副作用,抗肿瘤药物的临床生物活性和治疗剂量受到严重限制。纳米药物递送系统为克服小分子抗癌药物的缺点提供了一种出色的策略。
在此,我们分别通过离子交联和乳化交联制备了N,O-羧甲基壳聚糖奥沙利铂纳米粒(CMCS-OXE NPs)和N,O-羧甲基壳聚糖白藜芦醇纳米粒(CMCS-Res NPs)。
结果显示,CMCS-OXE NPs的包封率高达60%,粒径约为190.0 nm,CMCS-Res NPs的包封率高达65%,粒径约为164.2 nm。两种纳米粒联合处理比游离药物或单独的任何一种纳米粒均表现出更显著的抗结肠癌活性。在体内实验中,联合纳米粒处理的抑制效率比游离药物或单独的任何一种纳米粒都要强得多。
总体而言,将奥沙利铂和白藜芦醇组合成纳米药物递送系统似乎是一种有前景的结直肠癌(CRC)治疗策略。