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用于转移性乳腺癌治疗的HER-2受体和αvβ3整合素双配体表面功能化脂质体

HER-2 Receptor and αvβ3 Integrin Dual-Ligand Surface-Functionalized Liposome for Metastatic Breast Cancer Therapy.

作者信息

Arya Dilip Kumar, Deshpande Hemali, Kumar Ashish, Chidambaram Kumarappan, Pandey Prashant, Anjum Shabnam, Deepak Payal, Kumar Vikas, Kumar Santosh, Pandey Giriraj, Srivastava Saurabh, Rajinikanth Paruvathanahalli Siddalingam

机构信息

Department of Pharmaceutical Sciences, Babasaheb Bhimrao Ambedkar University, Lucknow 226025, India.

Department of Anatomy, College of Medicine, King Khalid University, Abha 61421, Saudi Arabia.

出版信息

Pharmaceutics. 2024 Aug 27;16(9):1128. doi: 10.3390/pharmaceutics16091128.

Abstract

Human epidermal growth factor receptor-2 (HER2)-positive breast cancer metastasis remains the primary cause of mortality among women globally. Targeted therapies have revolutionized treatment efficacy, with Trastuzumab (Trast), a monoclonal antibody, targeting HER2-positive advanced breast cancer. The tumor-homing peptide iRGD enhances the intratumoral accumulation and penetration of therapeutic agents. Liposomes serve as versatile nanocarriers for both hydrophilic and hydrophobic drugs. Gefitinib (GFB) is a potential anticancer drug against HER2-positive breast cancer, while Lycorine hydrochloride (LCH) is a natural compound with anticancer and anti-inflammatory properties. This study developed TPGS-COOH-coated liposomes co-loaded with GFB and LCH, prepared by the solvent injection method, and surface-functionalized with Trast and iRGD. The dual surface-decorated liposomes (DSDLs) were characterized for their particle size (PS), polydispersity index (PDI), zeta potential (ZP), surface chemistry, surface morphology, and their crystallinity during in-vitro drug release, drug encapsulation, and in-vitro cell line studies on SK-BR-3 and MDA-MB-231 breast cancer cells. The half-maximum inhibitory concentration (IC-50) values of single decorated liposomes (SDLs), iRGD-LP, and Trast-LP, as well as DSDLs (iRGD-Trast-LP) on SK-BR-3 cells, were 6.10 ± 0.42, 4.98 ± 0.36, and 4.34 ± 0.32 μg/mL, respectively. Moreover, the IC-50 values of SDLs and DSDLs on MDA-MB-231 cells were 15.12 ± 0.68, 13.09 ± 0.59, and 11.08 ± 0.48 μg/mL, respectively. Cellular uptake studies using confocal laser scanning microscopy (CLSM) showed that iRGD and Trast functionalization significantly enhanced cellular uptake in both cell lines. The wound-healing assay demonstrated a significant reduction in SDL and DSDL-treated MDA-MB-231 cell migration compared to the control. Additionally, the blood compatibility study showed minimal hemolysis (less than 5% RBC lysis), indicating good biocompatibility and biosafety. Overall, these findings suggest that TPGS-COOH-coated, GFB and LCH co-loaded, dual-ligand (iRGD and Trast) functionalized, multifunctional liposomes could be a promising therapeutic strategy for treating HER2-positive metastatic breast cancer.

摘要

人表皮生长因子受体2(HER2)阳性乳腺癌转移仍然是全球女性死亡的主要原因。靶向治疗彻底改变了治疗效果,曲妥珠单抗(Trast)作为一种单克隆抗体,可靶向HER2阳性晚期乳腺癌。肿瘤归巢肽iRGD可增强治疗药物在肿瘤内的蓄积和渗透。脂质体是亲水性和疏水性药物通用的纳米载体。吉非替尼(GFB)是一种潜在的抗HER2阳性乳腺癌抗癌药物,而盐酸石蒜碱(LCH)是一种具有抗癌和抗炎特性的天然化合物。本研究通过溶剂注入法制备了共载GFB和LCH的TPGS-COOH包被脂质体,并用Trast和iRGD进行表面功能化修饰。对双表面修饰脂质体(DSDLs)的粒径(PS)、多分散指数(PDI)、zeta电位(ZP)、表面化学、表面形态以及体外药物释放、药物包封和对SK-BR-3和MDA-MB-231乳腺癌细胞的体外细胞系研究中的结晶度进行了表征。单修饰脂质体(SDLs)、iRGD-LP和Trast-LP以及DSDLs(iRGD-Trast-LP)对SK-BR-3细胞的半数抑制浓度(IC-50)值分别为6.10±0.42、4.98±0.36和4.34±0.32μg/mL。此外,SDLs和DSDLs对MDA-MB-231细胞的IC-50值分别为15.12±0.68、13.09±0.59和11.08±0.48μg/mL。使用共聚焦激光扫描显微镜(CLSM)进行的细胞摄取研究表明,iRGD和Trast功能化显著增强了两种细胞系中的细胞摄取。伤口愈合试验表明,与对照组相比,SDL和DSDL处理的MDA-MB-231细胞迁移显著减少。此外,血液相容性研究显示溶血极少(红细胞裂解率低于5%),表明具有良好的生物相容性和生物安全性。总体而言,这些发现表明,TPGS-COOH包被、共载GFB和LCH、双配体(iRGD和Trast)功能化的多功能脂质体可能是治疗HER2阳性转移性乳腺癌的一种有前景的治疗策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fc0d/11435421/130653664538/pharmaceutics-16-01128-sch001.jpg

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