Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Anwar Siraj Daud"'
Publikováno v:
International Journal of Applied Pharmaceutics. :230-235
Objective: A randomized, open-label, balanced, two-treatment, two-period, two-sequence, single-dose, crossover bioequivalence study comparing Rizatriptan 10 mg Orally Disintegrating Strips (ODS, test) with that of established Oral Lyophilisate Rizatr
Publikováno v:
International Journal of Applied Pharmaceutics. :233-238
Objective: The present research work aims to develop a microemulsion loaded sublingual film for rapid absorption of fentanyl citrate in transient breakthrough pain. Methods: The Fentanyl citrate microemulsion loaded sublingual film was prepared using
Publikováno v:
International Journal of Applied Pharmaceutics. :127-135
Objective: The present research work aims to develop an abuse deterrent rapidly dissolving buprenorphine microemulsion loaded sublingual film for the treatment of breakthrough pain. Methods: The Buprenorphine microemulsion loaded sublingual films wer
Publikováno v:
International Journal of Applied Pharmaceutics. :230-235
Objective: The objective of the proposed work was to study the effect of various formulation and process parameters of solvent casting method on the physical and chemical stability of Ketorolac Tromethamine (KT) in the orally dissolving film dosage f
Autor:
Anwar Siraj Daud, Nidhi Sapkal
Publikováno v:
Nutraceuticals in Brain Health and Beyond ISBN: 9780128205938
The incidence of neurological disorders, especially Alzheimer disease (AD), is directly linked to increased age. There are several herbal drugs that have promising ability to treat AD and other neurological disorders but lack clinical efficacy due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8850e7c1f6cdf32f33de7a29f815e872
https://doi.org/10.1016/b978-0-12-820593-8.00024-0
https://doi.org/10.1016/b978-0-12-820593-8.00024-0
Autor:
Emad A.S. Al-Dujaili, Augustine Amalraj, Edward A. Armstrong, Zahra Ayati, Vladimir Badmaev, Arun Balakrishnan, Sharmistha Banerjee, Sarah Benson, Bharathi Bethapudi, Yves Bureau, Autumn Carriere, Brendan Casola, Zack Cernovsky, Nehru Sai Suresh Chalichem, Divya Chandradhara, Dennis Chang, Kaustubh S. Chaudhari, Simon S. Chiu, John Copen, Dezső Csupor, Hema Sharma Datta, Anwar Siraj Daud, Preeticia Dkhar, Sayanta Dutta, Seyed Ahmad Emami, Neha Garg, Sarah Gauci, Dilip Ghosh, Rohit Ghosh, Souvik Ghosh, Sumit Ghosh, Sreeraj Gopi, Gilles J. Guillemin, Swati Haldar, Marina Henein, Christine A. Houghton, Mariwan Husni, Satyajyoti Kanjilal, Diana Karamacoska, Chandra Kant Katiyar, Mostafa Khairy, Zahra Khazaeipool, Kamil Kuca, Viney Kumar, Zeenat Ladak, Debrupa Lahiri, Ed Lui, Helen Macpherson, Laura Martin, Bradley J. McEwen, Abhijeet Morde, Javad Mottaghipisheh, Deepak Mundkinajeddu, Sasikumar Murugan, Avinash Narwaria, Ruchong Ou, Muralidhara Padigaru, Bhushan Patwardhan, Naomi Perry, Andrew Pipingas, Pradeep Kumar Prajapati, Divya Purusothaman, Hana Raheb, Preeti Rathi, Frank Rosenfeldt, Renee Rowsell, Partha Roy, Saakshi Saini, Nidhi Prakash Sapkal, Frank Schoenlau, Andrew Scholey, Mujeeb Shad, Ramesh Sharma, Rohit Sharma, Vineet Sharma, Siddhansh Shrivastava, Weam Sieffien, Parames C. Sil, Ruby Sound, Angela V.E. Stockton, Con Stough, Ramesh Teegala, Kristen Terpstra, Prasad Arvind Thakurdesai, Barbara Tóth, Josh Varghese, Deepanshu Verma, Nikhil Verma, W.A.L. Chandrasiri Waliwita, David J. White, Michel Woodbury-Farina, Jay Kant Yadav, Jerome Y. Yager, Lauren M. Young, Andrea Zangara
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::48ea4264e99ccc1ae4f20c899adc0542
https://doi.org/10.1016/b978-0-12-820593-8.01002-8
https://doi.org/10.1016/b978-0-12-820593-8.01002-8
Publikováno v:
Journal of Applied Pharmaceutical Science. :159-169
Objective: Development and validated of a simple, selective RP-HPLC method for the determination of buprenorphine hydrochloride in pharmaceutical microemulsion formulation. A forced degradation study of developed formulation was carried out in accord
Publikováno v:
Asian Journal of Pharmaceutical and Clinical Research. 11:357
Objective: The objective of the study was to develop and validate new, simple, and selective reverse-phase–high-performance liquid chromatography (RP-HPLC) method for the quantitative determination of Dabigatran Etexilate (DE) and its impurities in