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作者:Effionora Anwar , Tahmida Diazputri Utami , Delly Ramadon
来源:[J].Asian Journal of Pharmaceutical and Clinical Research, 2017, Vol.10 (8), pp.294-298IAS
摘要:Objective: The aim of this study was to increase penetration of EGCG from green tea leaves extract (Camellia sinensis L. Kuntz) through the skin by formulating them into a transfersomal gel.Methods: Transfersomes were prepared by thin-layer hydration method, with different c...
作者:Effionora Anwar , Retnosari Andrajati
来源:[J].International Journal of Pharmacy and Pharmaceutical Sciences, 2014, Vol.7 (1), pp.124-129IAS
摘要:Objective: The objective of this research was to co-process via spray dry tablet excipients in the formulation of orodispersible tablet (ODT) containing Luffa acutangula (L) Roxb fruit aqueous extract (LAE) which were prepared by direct compression method.Methods: The excipients ...
作者:Kurnia Sari Setio Putri , Silvia Surini , Effionora Anwar
来源:[J].Asian Journal of Pharmaceutical and Clinical Research, 2013, Vol.6 (3), pp.62-66IAS
摘要:This present study was intended to expand utilization of starch as transdermal film-forming excipient. In the previous study, starch have been physically and chemically modified through complete pregelatinization and phthalatization process in aqueous-alkaline medium (pH 8-1...
作者:Effionora Anwar , Dyah Ayu Ratna Yulianti , Kurnia Sari Setio Putri
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.376-380IAS
摘要:Objective: This study aimed to determine the stability of microspheres of Sargassum plagyophyllum (brown seaweed) after preparation using spraydrying with maltodextrin DE 10–15 and during drying and storage.Methods: Aqueous extracts of brown seaweed were formulated into micr...
作者:Effionora Anwar , Delly Ramadon , Ghina Desviyanti Ardi
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.299-302IAS
摘要:Objective: This study aimed to formulate a transethosome cream (TEC) to increase skin penetration of epigallocatechin gallate (EGCG) in green tealeaf extract and evaluate their physicochemical characteristics and skin penetration capacity.Methods: Transethosomes were prepare...
作者:Effionora Anwar , Jeanetha Inees , Delly Ramadon
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.221-224IAS
摘要:Objective: This study aimed to formulate the epigallocatechin gallate (EGCG) from green tea into ethosomes and measure the resulting increases inskin penetration using a rat model.Methods: Ethosomes were formulated using ethanol concentrations of 25% (F1), 30% (F2), and 35% ...
作者:Effionora Anwar , Hilmia Erianto , Kurnia Sari Setio Putri
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.348-353IAS
摘要:Objective: The aim of this study was to prepare powder from liquid extract with maltodextrin dextrose equivalent 10–15 as a stabilizer using a freezedryingmethod to maintain stability during drying process and extend storage time.Methods: Powders were prepared for four formu...
作者:Effionora Anwar , Putri Amalia Handayani
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.211-215IAS
摘要:Objective: The aim of this study was to prepare transfersome-loaded microspheres which had good characteristics and physicochemical stability toincrease bioavailability of the polyphenol component of green tea leaf extract in the body.Methods: Transfersomes were prepared usi...
作者:Delly Ramadon , Seshiana Sebti Pramesti , Effionora Anwar
来源:[J].International Journal of Applied Pharmaceutics, 2017, Vol.9 (5), pp.91-96IAS
摘要:Objective: The aim of this study was to increase penetration of epigallocatechin gallate (EGCG) from the extract using transethosomal gel.Methods: Transethosomes (TE) formulae were made using thin layer hydration method with different concentration of green tea extract which...
作者:... Kurnia Ss Putri , Hayun Hayun , Effionora Anwar
来源:[J].International Journal of Applied Pharmaceutics, 2018, Vol.10 (1), pp.59-65IAS
摘要:Objective: This study was aimed to obtain a new excipient that can be used as a polymer matrix for the formulation of controlled release dosage forms.Methods: This study used coprocessing and crosslinking methods on amylose and xanthan gum (XG) to obtain a new excipient that...

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