Zobrazeno 1 - 10
of 79
pro vyhledávání: '"M. C. S. Subha"'
Publikováno v:
E-Journal of Chemistry, Vol 7, Iss 3, Pp 745-750 (2010)
The title compounds (7a-h) were prepared by esterification of indole-5-carboxylic acid (1) and subsequent treatment with hydrazine hydrate in methanol via the hydrazide (3). Finally hydrazide (3) condensed with different substituted aldol (6) in acet
Externí odkaz:
https://doaj.org/article/7851932c96cc44d882347e4b4f2439ea
Autor:
S. Bharathi, M. C. S. Subha
Publikováno v:
Russian Journal of Physical Chemistry A. 95:S201-S208
Publikováno v:
Journal of Pharmaceutical Analysis, Vol 11, Iss 2, Pp 191-199 (2021)
Journal of Pharmaceutical Analysis
Journal of Pharmaceutical Analysis
The aim of the present work is fabrication of dual cross linked sodium alginate (SA)/montmorillonite (MMT) microbeads as a potential drug vehicle for extended release of curcumin (CUR). The microbeads were prepared using in situ ion-exchange followed
Publikováno v:
International Journal of Applied Pharmaceutics. :249-257
Objective: The aim of the present work is to fabricate curcumin (CUR) encapsulated microbeads in the polymer matrix of sodium alginate (SA)/poly(vinylpyrrolidone)-co-vinyl acetate (PVP-co-VAc) intercalated with magnetite nanoparticles (MNPs) using gl
Publikováno v:
Polymers and Polymer Composites. 29:163-175
This article reports the fabrication of pH-sensitive microbeads from sodium alginate (SA) and modified karaya gum (KG). KG was modified by graft copolymerization using 2-hydroxyethyl methacrylate (2-HEMA) through in situ free radical polymerization r
Autor:
T. Jithendra, B. Mallikarjuna, O. Sreekanth Reddy, C. Madhavi, K. Chowdoji Rao, M. C. S. Subha
Publikováno v:
International Journal of Applied Pharmaceutics. :71-80
Objective: The aim of the present study was to fabricate and evaluate the drug release studies using Sodium Alginate (SA) and Gelatin (GE) microbeads intercalated with Kaolin (KA) nanoclay for sustained release of D-Penicillamine (D-PA). Methods: Sod
Publikováno v:
Tetrahedron. 75:874-887
A Suzuki-Miyaura cross coupling, followed by triphenylphosphine mediated Cadogan reductive cyclization sequence provided efficient access to a series of carbazole alkaloids. In the present work, this approach was applied to the total synthesis of muk
Autor:
Khadijatul Qubra, M. C. S. Subha, K. Chowdoji Rao, S. S. Kuthar, Pamela Sinha, Krystal M. Rivera-Rodríguez, B. Mallikarjuna, K. Pallavi, Leticia Eligio-García, Ramatoulaye Hamidou Lazoumar, Márió Gajdács, Ruchika Nandha, V. V. Kovalev, Saad Mohamed Hussein Ayoub, T. I. Ivko, Moustapha Mahamane Lamine, V. Krishnaveni, Elida Pontifez-Pablo, S. V. Spyrydonov, Sharma Khemchand, Muna Abdel Latif Khalil, Chinky Goyal, L. O. Bobrytska, M. G. Hogade, Ibrahim Maman Laminou, L. Iakovlieva, Bisu Singh, Andrea Foglio Bonda, K. Madhusudana Rao, Daou Maman, T. A. Germanyuk, Lorella Giovannelli, Aminata Iro, Lorena Segale, Raúl H Morales-Borges, A. O. Adebola Yusuf, Kantha D. Arunachalam, Harouna Amadou Mahaman Laouali, Olena Koshova, Gupta Arun Kumar, Enedina Jiménez-Cardoso, Salud Pérez-Gutiérrez, Mahamadou Doutchi, Ibrahim Alkassoum, Seydou Maiguizo, Anatoly Gordienko, N. A. Gordzievska, O. Tkachova, Harpal Singh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::47509482d58d1f364bce9ba33974e29b
https://doi.org/10.9734/bpi/tprd/v2
https://doi.org/10.9734/bpi/tprd/v2
Publikováno v:
Journal of synchrotron radiation. 27(Pt 1)
It is crucial to develop an environmentally friendly and low-cost method to treat industrial effluent that contains soluble dyes and microbes. Most of the photocatalysts have been studied using an external light source that increases the cost of the
Autor:
Kashayi Chowdojirao, Chintha Madhavi, Areti Parandhama, M. C. S. Subha, Palla Kumara Babu, Yeggada Maruthi, Guruguntla Nagarjuna
Publikováno v:
Journal of Applied Pharmaceutical Science. :011-019
Flutamide (FLT) is a potent non-steroidal antiandrogen drug primarily used in palliative treatment of prostate cancer that inhibits androgen uptake and / or nuclear binding of androgen in target tissue, the present study gives, the experimental resul