Journal of microencapsulation · 2026
Nanofabrication of shikonin accelerates the wound healing potential in diabetic rats via downregulation of MMP-9: in vitro/in vivo pharmacological validation and in silico molecular dynamic approach.
СтатьяНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Kaur Kirandeep, Monga Aditi, Mehra Anshula, Singh Atamjit, Kaur Sukhraj, Bedi Neena
Аннотация
BACKGROUND: Diabetic burn wounds are challenging comorbid conditions to heal, hence shikonin, a traditional phytoconstituent was nanofabricated in the present study. This study is the continuation of our previously published work including shikonin-loaded nanoemulsion against wound pathogens.
OBJECTIVE: Current work aims to further prepare electrospun scaffolds to promote wounded skin regeneration.
METHODS: Studies including DLS, ATR, XRD, SEM were used to assess pharmaceutical stability of system. In vivo model, western blotting (protein expression of MMP-9), soluble collagen and MMP-9 ELISA kit assays, molecular docking and simulations studies were used to evaluate pharmacodynamic stability.
RESULTS: The developed scaffolds exhibited chemical stability, improved aqueous solubility with average diameter of 235 ± 23 nm. The wound area got remarkably decreased (4.923 ± 0.935%) with high collagen content (88.515 ± 2.23%) and lower MMP-9 content (6.726 ± 0.820%) than the comparable groups.
CONCLUSION: The present study displayed the developed system with remarkable wound healing potential.
OBJECTIVE: Current work aims to further prepare electrospun scaffolds to promote wounded skin regeneration.
METHODS: Studies including DLS, ATR, XRD, SEM were used to assess pharmaceutical stability of system. In vivo model, western blotting (protein expression of MMP-9), soluble collagen and MMP-9 ELISA kit assays, molecular docking and simulations studies were used to evaluate pharmacodynamic stability.
RESULTS: The developed scaffolds exhibited chemical stability, improved aqueous solubility with average diameter of 235 ± 23 nm. The wound area got remarkably decreased (4.923 ± 0.935%) with high collagen content (88.515 ± 2.23%) and lower MMP-9 content (6.726 ± 0.820%) than the comparable groups.
CONCLUSION: The present study displayed the developed system with remarkable wound healing potential.