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使用可生物降解脂质纳米颗粒增强吉非替尼和阿扎胞苷的联合递送用于治疗转移性耐药肺癌

Enhanced Codelivery of Gefitinib and Azacitidine for Treatment of Metastatic-Resistant Lung Cancer Using Biodegradable Lipid Nanoparticles.

作者信息

Elzayat Ehab M, Sherif Abdelrahman Y, Nasr Fahd A, Attwa Mohamed W, Alshora Doaa H, Ahmad Sheikh F, Alqahtani Ali S

机构信息

Department of Pharmaceutics, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

Department of Pharmacognosy, College of Pharmacy, King Saud University, P.O. Box 2457, Riyadh 11451, Saudi Arabia.

出版信息

Materials (Basel). 2023 Jul 30;16(15):5364. doi: 10.3390/ma16155364.

DOI:10.3390/ma16155364
PMID:37570067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10419431/
Abstract

Lung cancer is a formidable challenge in clinical practice owing to its metastatic nature and resistance to conventional treatments. The codelivery of anticancer agents offers a potential solution to overcome resistance and minimize systemic toxicity. The encapsulation of these agents within nanostructured lipid carriers (NLCs) provides a promising strategy to enhance lymphatic delivery and reduce the risk of relapse. This study aimed to develop an NLC formulation loaded with Gefitinib and Azacitidine (GEF-AZT-NLC) for the treatment of metastatic-resistant lung cancer. The physicochemical properties of the formulations were characterized, and in vitro drug release was evaluated using the dialysis bag method. The cytotoxic activity of the GEF-AZT-NLC formulations was assessed on a lung cancer cell line, and hemocompatibility was evaluated using suspended red blood cells. The prepared formulations exhibited nanoscale size (235-272 nm) and negative zeta potential values (-15 to -31 mV). In vitro study revealed that the GEF-AZT-NLC formulation retained more than 20% and 60% of GEF and AZT, respectively, at the end of the experiment. Hemocompatibility study demonstrated the safety of the formulation for therapeutic use, while cytotoxicity studies suggested that the encapsulation of both anticancer agents within NLCs could be advantageous in treating resistant cancer cells. In conclusion, the GEF-AZT-NLC formulation developed in this study holds promise as a potential therapeutic tool for treating metastatic-resistant lung cancer.

摘要

由于肺癌具有转移性且对传统治疗有抗性,因此它在临床实践中是一项艰巨的挑战。联合递送抗癌药物为克服抗性和将全身毒性降至最低提供了一种潜在的解决方案。将这些药物封装在纳米结构脂质载体(NLCs)中为增强淋巴递送和降低复发风险提供了一种有前景的策略。本研究旨在开发一种负载吉非替尼和阿扎胞苷的NLC制剂(GEF-AZT-NLC)用于治疗转移性耐药肺癌。对制剂的理化性质进行了表征,并使用透析袋法评估了体外药物释放。评估了GEF-AZT-NLC制剂对肺癌细胞系的细胞毒性活性,并使用悬浮红细胞评估了血液相容性。制备的制剂呈现纳米级尺寸(235-272 nm)和负的zeta电位值(-15至-31 mV)。体外研究表明,在实验结束时,GEF-AZT-NLC制剂分别保留了超过20%的吉非替尼和60%的阿扎胞苷。血液相容性研究证明了该制剂用于治疗的安全性,而细胞毒性研究表明,将两种抗癌药物封装在NLCs中在治疗耐药癌细胞方面可能具有优势。总之,本研究开发的GEF-AZT-NLC制剂有望成为治疗转移性耐药肺癌的潜在治疗工具。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/291c64451355/materials-16-05364-g011.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/ac405be07bec/materials-16-05364-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/214aab0640fd/materials-16-05364-sch001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/9ac60f60aa79/materials-16-05364-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/d465ee395e18/materials-16-05364-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/2940d6e8dd0f/materials-16-05364-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/7f92bc9b3b3a/materials-16-05364-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/302005702094/materials-16-05364-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/c51bb4517b64/materials-16-05364-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/85ad/10419431/291c64451355/materials-16-05364-g011.jpg

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