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GRP78 靶向载多柔比星纳米液滴联合超声:一种用于去势抵抗性前列腺癌的潜在新型治疗策略。

GRP78-targeted and doxorubicin-loaded nanodroplets combined with ultrasound: a potential novel theranostics for castration-resistant prostate cancer.

机构信息

Department of Ultrasound, Qilu Hospital of Shandong University, Jinan, China.

出版信息

Drug Deliv. 2022 Dec;29(1):203-213. doi: 10.1080/10717544.2021.2023698.

DOI:10.1080/10717544.2021.2023698
PMID:34985396
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8741251/
Abstract

The construction of multifunctional oncotherapy nanoplatforms that combine diagnosis and treatment remains challenging. Nanodroplets (NDs), which simultaneously enhance ultrasound imaging and therapeutic effects, are a potential strategy for non-invasive drug delivery. To achieve the goals of precise medicine, novel SP94 peptide-modified and doxorubicin-loaded ultrasonic NDs (SP94-DOX-NDs) for castration-resistant prostate cancer (CRPC) targeting and treatment were constructed in this study. The characteristics, contrast-enhanced ultrasound imaging (CEUI), targeting ability to glucose-regulated protein 78 (GRP78)-overexpressing CRPC and anticancer effect of the SP94-DOX-NDs were assessed. The desired SP94-NDs were successfully prepared using the nanoemulsification method using a certain proportion of SP94-PEG-chitosan, perfluoropentane (PFP), Tween 20, and lecithin. SP94-NDs with a size of ∼300 nm showed great biocompatibility and CEUI ability. Compared with blank NDs, SP94-NDs exhibited higher tumor-specific targeting ability due to conjugation between the SP94 peptide and GRP78-overexpressing 22RV1 cells. Most importantly, and investigations showed that SP94-DOX-NDs combined with ultrasound could specifically deliver DOX into 22RV1 cells and thereby demonstrated a stronger anticancer effect than DOX-NDs and DOX. Thus, SP94-DOX-NDs may provide an efficient approach for the real-time imaging of tumors and triggered, accurate drug delivery to tumors.

摘要

多功能肿瘤治疗纳米平台的构建,将诊断和治疗相结合,仍然具有挑战性。纳米液滴(NDs)同时增强超声成像和治疗效果,是一种潜在的非侵入性药物传递策略。为了实现精准医学的目标,本研究构建了新型 SP94 肽修饰和多柔比星负载的超声 NDs(SP94-DOX-NDs),用于针对去势抵抗性前列腺癌(CRPC)的靶向治疗。评估了 SP94-DOX-NDs 的特性、超声增强成像(CEUI)、对葡萄糖调节蛋白 78(GRP78)过表达的 CRPC 的靶向能力和抗癌效果。采用纳米乳化法,使用一定比例的 SP94-PEG-壳聚糖、全氟戊烷(PFP)、吐温 20 和卵磷脂,成功制备了所需的 SP94-NDs。粒径约为 300nm 的 SP94-NDs 具有良好的生物相容性和 CEUI 能力。与空白 NDs 相比,SP94-NDs 由于 SP94 肽与 GRP78 过表达的 22RV1 细胞之间的缀合,表现出更高的肿瘤特异性靶向能力。最重要的是,体内和体外研究表明,SP94-DOX-NDs 联合超声能将 DOX 特异性递送至 22RV1 细胞,从而表现出比 DOX-NDs 和 DOX 更强的抗癌效果。因此,SP94-DOX-NDs 可能为肿瘤的实时成像和触发、精确的肿瘤药物输送提供一种有效的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/48fa4d4a5d9e/IDRD_A_2023698_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/b8d323bd0281/IDRD_A_2023698_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/1521e353370c/IDRD_A_2023698_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/3ccd27a33818/IDRD_A_2023698_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/78077caa9311/IDRD_A_2023698_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/bd4da2ae05ed/IDRD_A_2023698_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/48fa4d4a5d9e/IDRD_A_2023698_F0006_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/b8d323bd0281/IDRD_A_2023698_F0001_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/1521e353370c/IDRD_A_2023698_F0002_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/3ccd27a33818/IDRD_A_2023698_F0003_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/78077caa9311/IDRD_A_2023698_F0004_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/bd4da2ae05ed/IDRD_A_2023698_F0005_C.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b9d/8741251/48fa4d4a5d9e/IDRD_A_2023698_F0006_C.jpg

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