Zobrazeno 1 - 10
of 31
pro vyhledávání: '"Damineni, Saritha"'
Publikováno v:
Research Journal of Pharmacy and Technology. :2062-2068
Microemulsions, by virtue of their lipophilic nature and low globule size, are widely explored as a delivery system to enhance uptake across mucosa. The main aim of the present investigation is to develop and in vitro characterization of intra nasal
Autor:
Damineni Saritha, Penjuri Subhash Chandra Bose, Poreddy Srikanth Reddy, Grandhi Madhuri, Ravouru Nagaraju
Publikováno v:
Brazilian Journal of Pharmaceutical Sciences, Vol 48, Iss 4, Pp 683-690 (2012)
Naproxen, an anti-inflammatory drug, exhibits poor aqueous solubility, which limits the pharmacological effects. The present work was carried out to study the effect of agglomeration on micromeritic properties and dissolution. Naproxen agglomerates w
Externí odkaz:
https://doaj.org/article/4631506b44ae4ff790546ce210c87ac1
Autor:
P Srikanth Reddy, Damineni Saritha, P. Subhash Chandra Bose, Gokul Subramanian Ravi, Vuppula Sruthi
Publikováno v:
International Journal of Pharma Research and Health Sciences. 7:3105-10
Autor:
Damineni Saritha, P Srikanth Reddy, V. Alagarsamy, Gokul Subramanian Ravi, P. Subhash Chandra Bose
Publikováno v:
International Journal of Medical and Biomedical Studies. 5
Transdermal drug delivery is an alternative route for systemic drug delivery which minimizes the absorption and increases the bioavailability. The main objective of the present work was to develop a suitable matrix type transdermal drug delivery syst
Autor:
PENJURI, Subhash Chandra Bose1 penjurisubhash@gmail.com, DAMINENI, Saritha2, RAVOURU, Nagaraju3, POREDDY, Srikanth Reddy1
Publikováno v:
Turkish Journal of Pharmaceutical Sciences. 2017, Vol. 14 Issue 2, p108-119. 12p. 9 Charts, 8 Graphs.
Publikováno v:
Recent Patents on Drug Delivery & Formulation. 10:235-244
Background: The objective of this investigation was to develop a self emulsifying drug delivery system (SEDDS) of naproxen, a poorly water soluble drug, which could improve its solubility and oral bioavailability. Methods: The recent patents on SEDDS
Publikováno v:
International Journal of Medical and Biomedical Studies. 3
The modern drug delivery system of hydrophobic drugs presents a main challenge because of the poor aqueous solubility of such compounds. Self emulsifying drug delivery systems (SEDDS) are usually used to enhance the bioavailability of hydrophobic dru
Publikováno v:
Research Journal of Pharmacy and Technology. 13:2954
The main purpose of the present review is to compile the recent literature with special focus on different aspects of Buccal drug delivery system (BDDS) that achieve significance place among novel drug deliveries. The main obstacles that drugs meet w
Publikováno v:
International Journal of Drug Delivery Technology. 8
The aim of the present work was to prepare floating tablets of galantamine HBr using sodium alginate and xanthan gum as matrix forming carriers. Galantamine HBr is used for the treatment of mild to moderate Alzheimer's disease and various other memor
Publikováno v:
International Journal of Pharmaceutical Sciences and Nanotechnology. 8:2715-2722
Self-emulsifying drug delivery systems (SEDDS) possess unparalleled potential in improving oral bioavailability of poorly water-soluble drugs. Following their oral administration, these systems rapidly disperse in gastrointestinal fluids, yielding mi