碳酸酐酶IX抑制剂和阿霉素共同递送是解决缺氧诱导的化疗耐药的有希望的方法。

IF 6.5 2区 医学 Q1 PHARMACOLOGY & PHARMACY
Muhammad Umair Amin, Sajid Ali, Muhammad Yasir Ali, Dominik C Fuhrmann, Imran Tariq, Benjamin S Seitz, Eduard Preis, Jana Brüßler, Bernhard Brüne, Udo Bakowsky
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引用次数: 0

摘要

肿瘤缺氧是肿瘤耐药的主要原因之一。在正常情况下,碳酸酐酶通常参与pH稳态,但在与缺氧密切相关的实体肿瘤中,碳酸酐酶IX (CA-IX)酶过表达,导致细胞外酸性环境。对于大多数弱碱性抗癌药物,包括阿霉素(Dox),在酸性环境中的电离限制了它们的细胞摄取,因此,肿瘤暴露在亚治疗浓度的药物下会产生化疗耐药性。本研究开发了一种由脂质体和介孔二氧化硅纳米颗粒(MSNPs)组成的联合给药系统,用于在缺氧条件下共同递送CA-IX酶抑制剂和Dox。MSNPs的独特结构具有较高的表面积,可用于提高Dox的载药量和缓释。此外,脂质体包被作为CA-IX酶抑制剂的第二装载位点的生物相容性提供了在孔打开处的把关作用,以避免药物过早释放。脂质包被MSNPs作为Dox和CA-IX抑制剂的共递送系统,在缺氧条件下对MDA-MB 231乳腺癌细胞具有协同细胞毒作用。这些发现保证了这种药物输送系统克服缺氧相关化疗耐药的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Co-delivery of carbonic anhydrase IX inhibitor and doxorubicin as a promising approach to address hypoxia-induced chemoresistance.

Co-delivery of carbonic anhydrase IX inhibitor and doxorubicin as a promising approach to address hypoxia-induced chemoresistance.

Co-delivery of carbonic anhydrase IX inhibitor and doxorubicin as a promising approach to address hypoxia-induced chemoresistance.

Co-delivery of carbonic anhydrase IX inhibitor and doxorubicin as a promising approach to address hypoxia-induced chemoresistance.

Hypoxia, an oxygen-deprived condition of the tumor, is one of the major reasons for resistance to chemotherapy. Carbonic anhydrases are generally involved in pH homeostasis in normal conditions, but in solid tumors having a strong relation with hypoxia, the carbonic anhydrase IX (CA-IX) enzyme is overexpressed and results in an extracellular acidic environment. For most weakly basic anticancer drugs, including doxorubicin (Dox), the ionization in an acidic environment limits their cellular uptake, and consequently, the tumor exposure to the drug at sub-therapeutic concentration comes out as chemoresistance. Herein, a combined drug delivery system of liposomes and mesoporous silica nanoparticles (MSNPs) was developed for the co-delivery of the CA-IX enzyme inhibitor and Dox in hypoxic condition. The unique structure of MSNPs with higher surface area was utilized for higher drug loading and sustained release of Dox. Additionally, the biocompatible nature of liposomal coating as a second loading site for the CA-IX enzyme inhibitor has provided gatekeeping effects at pore opening to avoid premature drug release. Lipid coated MSNPs as a co-delivery system for Dox and the CA-IX inhibitor have synergistic cytotoxic effects against MDA-MB 231 breast cancer cells in hypoxic conditions. These findings assure the potential of this drug delivery system to overcome hypoxia-related chemoresistance.

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来源期刊
Drug Delivery
Drug Delivery 医学-药学
CiteScore
11.80
自引率
5.00%
发文量
250
审稿时长
3.3 months
期刊介绍: Drug Delivery is an open access journal serving the academic and industrial communities with peer reviewed coverage of basic research, development, and application principles of drug delivery and targeting at molecular, cellular, and higher levels. Topics covered include all delivery systems including oral, pulmonary, nasal, parenteral and transdermal, and modes of entry such as controlled release systems; microcapsules, liposomes, vesicles, and macromolecular conjugates; antibody targeting; protein/peptide delivery; DNA, oligonucleotide and siRNA delivery. Papers on drug dosage forms and their optimization will not be considered unless they directly relate to the original drug delivery issues. Published articles present original research and critical reviews.
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