Heat-activated thermosensitive liposomal cisplatin (HTLC) results in effective growth delay of cervical carcinoma in mice

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• 作者：Yannan N. Dou^a ; Jinzi Zheng^b ; ^c ; Warren D. Foltz^b ; ^c ; Robert Weersink^c ; Naz Chaudary^d ; David A. Jaffray^b ; ^c ; ^e ; ^f ; ^g ; ^{david.jaffray@rmp.uhn.on.ca" class="auth_mail} ; Christine Allen^a ; ^b ; ^{cj.allen@utoronto.ca" class="auth_mail}
• 关键词：Thermosensitive liposome ; Cisplatin (CDDP) ; Gadoteridol (ProHance® ; Gd-HP-DO3A) ; Magnetic resonance (MR) imaging ; Laser heating ; Cervical cancer
• 刊名：Journal of Controlled Release
• 出版年：28 March, 2014
• 年：2014
• 卷：178
• 期：Complete
• 页码：69-78
• 全文大小：1253 K

文摘

Cisplatin (CDDP) has been identified as the primary chemotherapeutic agent for the treatment of cervical cancer, but dose limiting toxicity is a key issue associated with its clinical application. A suite of liposome formulations of CDDP has been developed in efforts to reduce systemic toxicity, but their therapeutic advantage over the free drug has been modest due to insufficient drug release at the tumor site. This report describes the development of a novel heat-activated thermosensitive liposome formulation containing CDDP (HTLC) designed to release approximately 90% of the loaded drug in less than 5 min under mild heating conditions (42 掳C). Physico-chemical characteristics of HTLC were assessed in terms of gel to liquid crystalline phase transition temperature (T_m), drug loading efficiency, particle size, and stability. The pharmacokinetic profile and biodistribution of HTLC in non-tumor-bearing mice were evaluated over a 24 h period. A sophisticated spatio-temporal elucidation of HTLC release in tumor-bearing mice was achieved by way of real-time monitoring using a magnetic resonance (MR) imaging protocol, wherein a custom-built laser-based conformal heat source was applied at the tumor volume to trigger the release of HTLC co-encapsulated with the MR contrast agent gadoteridol (Gd-HP-DO3A). MR thermometry (MRT) demonstrated that a relatively uniform temperature distribution was achieved in the tumor volume using the external laser-based heating setup. In mice bearing subcutaneously-implanted ME-180 cervical tumors, the combination of HTLC and heat resulted in a 2-fold increase in tumor drug levels at 1 h post-administration compared to HTLC without heating. Furthermore, the overall tumor accumulation levels for the HTLC groups (with and without heat) at 1 h post-injection were significantly higher than the corresponding free CDDP group. This translated into a significant improvement in therapeutic efficacy evaluated as tumor growth delay (p < 0.05) for the heated HTLC treatment group compared to the unheated HTLC, heated or unheated free CDDP, and saline groups. Overall, findings from this study demonstrate that a heat-activated, triggered release formulation of CDDP results in a significant enhancement in the therapeutic index of this drug.