Department of Gynecology, Shaoxing People's Hospital, Shaoxing Hospital, Zhejiang University School of Medicine, China.
Department of Pathology, Shaoxing People's Hospital, Shaoxing Hospital, Zhejiang University School of Medicine, China.
Biomed Pharmacother. 2018 Dec;108:565-573. doi: 10.1016/j.biopha.2018.09.039. Epub 2018 Sep 20.
Ovarian cancer is usually treated with transurethral resection or systemic chemotherapy in clinic. However, the development of drug resistance in ovarian cancer is frequently observed in ovarian cancer patients, leading to failure of tumor inhibition and recurrence. In this study, we aimed to efficiently reverse the drug resistance and enhance the anticancer effects by co-delivery of chemotherapeutic agents and multi-drugs resistant proteins inhibitor in ovarian cancer treatment.
The cell viability was measured by using MTT or flow cytometry (Annexin V/PI staining) under different culture conditions. Western blot was used to detect the expression of P-gp. We employed confocol to visualize the drug distribution under different culture systems. Using flow cytometry, we examined the drug absorption. MPEG-PLA was used to load chemotherapeutic drugs. We also applied mice model to evaluate the killing ability and side effects of free or methoxy poly (ethylene glycol)-poly (l-lactic acid) (MPEG-PLA) loaded drugs.
We found that pre-treatment of verapamil, a multi-drugs resistant proteins inhibitor, could efficiently reverse the drug resistant in ovarian cancer. To further improve the pharmacokinetics profiles and avoid the systemic toxicity caused by agents, we encapsulated verapamil and doxorubicin (DOX) by polymeric nanoparticles MPEG-PLA. Co-delivery of verapamil and DOX by nano-carrier revealed reduced drug resistance and enhanced anticancer effects compared with the free drug delivery. More importantly, accumulated drugs, prolonged drug circulation and reduced systemic were observed in nanoparticles encapsulation group.
Co-delivery of verapamil and chemotherapeutic drugs by MPEG-PLA efficiently reversed the drug resistance, resulting in enhanced anticancer effects along with reduced systemic toxicity, which provides potential clinical applications for drug resistant ovarian cancer treatment.
临床上通常采用经尿道电切术或全身化疗治疗卵巢癌。然而,卵巢癌患者常出现药物耐药,导致肿瘤抑制失败和复发。本研究旨在通过化疗药物和多药耐药蛋白抑制剂的共递送,有效逆转耐药并增强卵巢癌的治疗效果。
在不同的培养条件下,通过 MTT 或流式细胞术(Annexin V/PI 染色)测量细胞活力。Western blot 用于检测 P-gp 的表达。我们采用共聚焦显微镜观察不同培养系统下的药物分布。通过流式细胞术检测药物吸收。MPEG-PLA 用于载药。我们还应用小鼠模型评估游离或甲氧基聚乙二醇-聚(L-乳酸)(MPEG-PLA)载药的杀伤能力和副作用。
我们发现,多药耐药蛋白抑制剂维拉帕米预处理可有效逆转卵巢癌的耐药性。为了进一步改善药代动力学特性并避免因药物引起的全身毒性,我们将维拉帕米和阿霉素(DOX)包封在聚合物纳米粒 MPEG-PLA 中。与游离药物递送相比,纳米载体共递送维拉帕米和 DOX 可降低耐药性并增强抗癌效果。更重要的是,在纳米粒包封组中观察到药物蓄积增加、药物循环延长和全身毒性降低。
MPEG-PLA 共递送维拉帕米和化疗药物可有效逆转耐药性,增强抗癌效果,同时降低全身毒性,为耐药性卵巢癌的治疗提供了潜在的临床应用。