Department of Pharmaceutical Science, College of Pharmacy, University of Michigan, 428 Church Street, Ann Arbor, MI 48109-1065, USA.
Molecules. 2017 Aug 10;22(8):1322. doi: 10.3390/molecules22081322.
One of the main obstacles for cancer therapies is to deliver medicines effectively to target sites. Since stroma cells are developed around tumors, chemotherapeutic agents have to go through stroma cells in order to reach tumors. As a method to improve drug delivery to the tumor site, a prodrug approach for gemcitabine was adopted. Amino acid and dipeptide monoester prodrugs of gemcitabine were synthesized and their chemical stability in buffers, resistance to thymidine phosphorylase and cytidine deaminase, antiproliferative activity, and uptake/permeability in HFF cells as a surrogate to stroma cells were determined and compared to their parent drug, gemcitabine. The activation of all gemcitabine prodrugs was faster in pancreatic cell homogenates than their hydrolysis in buffer, suggesting enzymatic action. All prodrugs exhibited great stability in HFF cell homogenate, enhanced resistance to glycosidic bond metabolism by thymidine phosphorylase, and deamination by cytidine deaminase compared to their parent drug. All gemcitabine prodrugs exhibited higher uptake in HFF cells and better permeability across HFF monolayers than gemcitabine, suggesting a better delivery to tumor sites. Cell antiproliferative assays in Panc-1 and Capan-2 pancreatic ductal cell lines indicated that the gemcitabine prodrugs were more potent than their parent drug gemcitabine. The transport and enzymatic profiles of gemcitabine prodrugs suggest their potential for delayed enzymatic bioconversion and enhanced resistance to metabolic enzymes, as well as for enhanced drug delivery to tumor sites, and cytotoxic activity in cancer cells. These attributes would facilitate the prolonged systemic circulation and improved therapeutic efficacy of gemcitabine prodrugs.
癌症治疗的主要障碍之一是将药物有效地递送到靶位。由于基质细胞围绕肿瘤发育,因此化疗药物必须穿过基质细胞才能到达肿瘤。为了改善药物向肿瘤部位的递送,采用了吉西他滨的前药方法。合成了吉西他滨的氨基酸和二肽单酯前药,并比较了其母体药物吉西他滨在缓冲液中的化学稳定性、对胸苷磷酸化酶和胞苷脱氨酶的耐药性、抗增殖活性以及在 HFF 细胞中的摄取/渗透性。与缓冲液中的水解相比,所有吉西他滨前药在胰腺细胞匀浆中的激活都更快,提示存在酶促作用。所有前药在 HFF 细胞匀浆中均表现出很高的稳定性,与母体药物相比,对胸苷磷酸化酶的糖苷键代谢和胞苷脱氨酶的脱氨作用具有更强的耐药性。与吉西他滨相比,所有吉西他滨前药在 HFF 细胞中的摄取更高,透过 HFF 单层的渗透性更好,提示向肿瘤部位的递送更好。在 Panc-1 和 Capan-2 胰腺导管细胞系中的细胞增殖抑制测定表明,吉西他滨前药比其母体药物吉西他滨更有效。吉西他滨前药的转运和酶谱表明,它们具有延迟酶生物转化和增强对代谢酶的耐药性的潜力,以及增强向肿瘤部位的药物递送和癌细胞中的细胞毒性活性。这些特性将有助于延长吉西他滨前药的系统循环时间并提高治疗效果。