Abstract | BACKGROUND: METHODS AND RESULTS: Real-time infrared spectroscopy and rheological experiments showed that the SAE monomer with shear-thinning characteristics could polymerize rapidly into a transparent membrane. Cytotoxicity experiments in vitro showed that this system could elicit a long-term hemostatic effect. Tissue adhesion was also evaluated. The photo-stability of four delivered antifibrinolytic drugs ( 6-aminocaproic acid, ethylenediaminediacetic acid, tranexamic acid and p-(aminomethyl) benzoic acid) was tested by ultraviolet-photolysis experiments and illustrated by time-dependent density functional theory. Sustained-release experiments revealed that the formed film could be used as a drug carrier. Molecular docking and molecular dynamics were done to investigate the binding mechanism between hemostatic drugs as ligands and the human plasminogen kringle-1 (1HPK) as a target. CONCLUSION: It has been suggested that SAE with tranexamic acid could be a drug-release system of microchannel transport used in MIS. This system could tackle the dilemma of fluidity and adhesion in MIS. The photo-stable tranexamic acid was the most suitable drug according to its satisfactory binding energy, good photo-stability, and sustained release.
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Authors | Hong Huang, Houhe Liu, Hua Zhou, Zhiling Liang, Dandan Song, Yun Zhang, Wanqiu Huang, Xiaotian Zhao, Bo Wu, Guodong Ye, Yugang Huang |
Journal | Drug design, development and therapy
(Drug Des Devel Ther)
Vol. 13
Pg. 881-896
( 2019)
ISSN: 1177-8881 [Electronic] New Zealand |
PMID | 30880920
(Publication Type: Journal Article)
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Chemical References |
- Antifibrinolytic Agents
- Drug Carriers
- Ligands
- Plasminogen
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Topics |
- Antifibrinolytic Agents
(pharmacology)
- Density Functional Theory
- Drug Carriers
(chemistry)
- Drug Liberation
- Hemostasis
- Humans
- Kringles
(drug effects)
- Ligands
- Minimally Invasive Surgical Procedures
- Models, Molecular
- Plasminogen
(drug effects)
- Time Factors
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