Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Archana Sidagouda Patil"'
Autor:
Viresh Hanagandi, Archana Sidagouda Patil, Rajashree Shashidhar Masareddy, Panchaxari Mallappa Dandagi, Udaykumar Baburao Bolmal
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 56:94-102
Autor:
Anand Panchaxari Gadad, Archana Sidagouda Patil, Riya Hegde, Rajashree Shashidhar Masareddy, Uday Bolmal, Panchaxari Mallapa Dandagi
Publikováno v:
Turk J Pharm Sci
OBJECTIVES: Lovastatin is an antilipidemic drug that belongs to the class of statins that has poor oral bioavailability due to its low solubility and variable dissolution rate. The main aim of this study was to enhance the solubility and dissolution
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 55:374-382
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 55:s164-s175
Publikováno v:
Nanopharmaceutical Advanced Delivery Systems
Publikováno v:
Nanopharmaceutical Advanced Delivery Systems
Autor:
Panchaxari Mallappa Dandagi, Archana Sidagouda Patil, Uday Bolmal, Yashica Singh, Ananya Basu, Anand Panchaxari Gadad
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 54:954-962
Autor:
Umashri A Kokatanur, Udaykumar Bolmal, Archana Sidagouda Patil, Rajashree Shashidhar Masareddy, Cheran K
Background: The goal of this study was to develop a gastro retentive floating drug delivery system that would improve site specific activity, patient compliance and therapeutic efficacy.Methodology: Floating microspheres of Miglitol were formulated b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::af5d4f67b704a4524c3bde28f39038c0
https://doi.org/10.21203/rs.3.rs-826326/v1
https://doi.org/10.21203/rs.3.rs-826326/v1
Publikováno v:
Indian Journal of Pharmaceutical Education and Research. 53:s587-s595
Autor:
Rajashree Shashidhar Masareddy, Vedangi Tuencar, Archana Sidagouda Patil, Panchaxari Mallappa Dandagi, AP Gadad
Publikováno v:
Therapeutic delivery. 12(8)
Background: Nanostructured lipid carriers (NLCs) of fluconazole were prepared to improve permeability and thereby effective topical drug delivery. Materials and methods: NLCs were prepared and evaluated, and then the optimized NLC suspension was inco