Author/Authors :
Kalalinia, Fatemeh Mashhad University of Medical Sciences, Mashhad , Amiri, Nafise Department of Pharmaceutical Nanotechnology - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad , Mehrvarzian, Niloufar Department of Pharmaceutical Nanotechnology - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad , Fazly Bazzaz, Bibi Sedigheh Mashhad University of Medical Sciences, Mashhad , Iranshahi, Mehrdad Mashhad University of Medical Sciences, Mashhad , Shahroodi, Azadeh Department of Pharmaceutics - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad , Arabzadeh, Sepideh Mashhad University of Medical Sciences, Mashhad , Abbaspour, Mohammadreza Department of Pharmaceutics - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad , Badiee Aaval, Shapour Faculty of Traditional Medicine - Mashhad University of Medical Sciences, Mashhad , Movaffagh, Jebrail Department of Pharmaceutics - School of Pharmacy - Mashhad University of Medical Sciences, Mashhad
Abstract :
Objective(s): Potentially preventable death from uncontrolled hemorrhage clearly indicates the
importance of simple, fast and efficient ways to achieving hemostasis. The aim of this study was
to develop a topical formulation of green tea extract for reducing bleeding that can be helpful in
hemorrhage control.
Materials and Methods: Hydroalcoholic extract of green tea was isolated from Camellia sinensis and
formulated in polyvinyl alcohol (PVA) to achieve two concentrations of 2% and 4% v/v. Folin-Ciocalteau
assay was used to determine the total amount of tannins in extract. Rheological behavior of solutions was
investigated by measuring viscosity at shear rates of 0–200 sec−1. Quantitative and qualitative microbial limit
tests and minimum inhibitory concentration (MIC) assay were done. The effect of formulations on bleeding
time was evaluated in an animal model.
Results: The total amount of tannin in green tea extract was 3.8% w/w and addition of green tea
significantly increased the viscosity of PVA. The results of MIC assay showed that PVA could not
inhibit the growth of bacteria, while, 716 μg/ml of green tea and 2860 μg/ml of green tea/PVA 4%
inhibited the growth of Staphylococcus aureus and Pseudomonas aeruginosa. In an animal study both
2% and 4% formulations were able to stop hemorrhage approximately at an equal time compared
with tranexamic acid (TXA) 50 mg/ml as a control and the lowest bleeding time was 6.4±0.51 sec for
green tea/PVA 4%.
Conclusion: Based on our results, the topical formulation of green tea extract in PVA has a great
potential for anti-hemorrhage applications.
Keywords :
Bleeding , Green tea , Hemostasis , Polyvinyl alcohol , Tannin , Topical formulation