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水飞蓟宾/姜黄素负载白蛋白纳米粒经壳聚糖包被作为黏液吸入式递药系统,观察其在油酸诱导的肺损伤和体外 COVID-19 实验中的抗炎和抗 COVID-19 特性。

Silymarin/curcumin loaded albumin nanoparticles coated by chitosan as muco-inhalable delivery system observing anti-inflammatory and anti COVID-19 characterizations in oleic acid triggered lung injury and in vitro COVID-19 experiment.

机构信息

Nanomedicine group, Institute of Nanoscience and Nanotechnology, Kafrelsheikh University, 33516 Kafrelsheikh, Egypt.

出版信息

Int J Biol Macromol. 2022 Feb 15;198:101-110. doi: 10.1016/j.ijbiomac.2021.12.073. Epub 2021 Dec 28.

DOI:10.1016/j.ijbiomac.2021.12.073
PMID:34968533
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8712435/
Abstract

Respiratory infected by COVID-19 represents a major global health problem at moment even after recovery from virus corona. Since, the lung lesions for infected patients are still sufferings from acute respiratory distress syndrome including alveolar septal edema, pneumonia, hyperplasia, and hyaline membranes Therefore, there is an urgent need to identify additional candidates having ability to overcome inflammatory process and can enhance efficacy in the treatment of COVID-19. The polypenolic extracts were integrated into moeties of bovine serum albumin (BSA) and then were coated by chitosan as a mucoadhesion polymer. The results of interleukin-6, and c-reactive protein showed significant reduction in group treated by Encap. SIL + CUR (64 ± 0.8 Pg/μL & 6 ± 0.5 μg/μL) compared to group treated by Cham. + CUR (102 ± 0.8 Pg/μL & 7 ± 0.5 μg/μL) respectively and free capsules (with no any drug inside) (148 ± 0.6 Pg/μL & 10 ± 0.6 μg/μL) respectively. Histopathology profile was improved completely. Additionally, encapsulating silymarin showed anti-viral activity in vitro COVID-19 experiment. It can be summarized that muco-inhalable delivery system (MIDS) loaded by silymarin can be used to overcome inflammation induced by oleic acid and to overcome COVID-19.

摘要

感染 COVID-19 的呼吸道问题目前仍是一个全球性的主要健康问题,即使在从冠状病毒中康复之后也是如此。由于感染患者的肺部病变仍然患有急性呼吸窘迫综合征,包括肺泡隔水肿、肺炎、增生和透明膜,因此,迫切需要确定其他具有克服炎症过程的能力并能提高 COVID-19 治疗效果的候选物。多酚提取物整合到牛血清白蛋白 (BSA) 的摩尔中,然后用壳聚糖作为粘膜粘附聚合物进行涂层。白细胞介素 6 和 C 反应蛋白的结果表明,与 Cham. + CUR(分别为 102 ± 0.8Pg/μL 和 7 ± 0.5μg/μL)组相比,Encap. SIL + CUR 组(64 ± 0.8Pg/μL 和 6 ± 0.5μg/μL)显著减少,而与无任何药物的游离胶囊(分别为 148 ± 0.6Pg/μL 和 10 ± 0.6μg/μL)相比,结果也有显著减少。组织病理学特征得到了完全改善。此外,包封的水飞蓟素在 COVID-19 体外实验中显示出抗病毒活性。可以总结的是,负载水飞蓟素的粘膜可吸入给药系统 (MIDS) 可用于克服油酸诱导的炎症和克服 COVID-19。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/a4674607b0fd/gr10_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/7431b106116f/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/14aedc3df459/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/d8e041b7a0af/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/f4b7649c78b4/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/ba968f4a7309/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/5415da093008/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/c0be57d03e61/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/9b0001af4ba9/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/b086396ec2a8/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/a4674607b0fd/gr10_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/7431b106116f/gr1_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/14aedc3df459/gr2_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/d8e041b7a0af/gr3_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/f4b7649c78b4/gr4_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/ba968f4a7309/gr5_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/5415da093008/gr6_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/c0be57d03e61/gr7_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/9b0001af4ba9/gr8_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/b086396ec2a8/gr9_lrg.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0f34/8712435/a4674607b0fd/gr10_lrg.jpg

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