Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fiza Ur Rehman"'
Autor:
Fiza ur Rehman, Syeda Sohaila Naz, Muhammad Junaid Dar, Annum Malik, Maimoona Qindeel, Francesco Baino, Fazli Wahid, Abbas Rahdar, Saeeda Munir, Sara Qaisar, Kifayat Ullah Shah, Mahtab Razlansari
Publikováno v:
Iranian Journal of Materials Science and Engineering, Vol 19, Iss 2, Pp 1-30 (2022)
Neoplastic cells have co-opted inflammatory receptors and signaling molecules that potentiate inflammation. Activated inflammatory pathways lead to neo-angiogenesis, lymph-angiogenesis, immunosuppression, tumor growth, proliferation and metastasis. T
Externí odkaz:
https://doaj.org/article/75bf314cb6224f8fbe44c5ed13fedeeb
Autor:
Fiza Ur Rehman, Arshad Farid, Shefaat Ullah Shah, Muhammad Junaid Dar, Asim Ur Rehman, Naveed Ahmed, Sheikh Abdur Rashid, Irfan Shaukat, Muddaser Shah, Ghadeer M. Albadrani, Mohamed Kamel, Ahmed E. Altyar, Mohamed M. Abdel-Daim, Kifayat Ullah Shah
Publikováno v:
Pharmaceuticals, Vol 15, Iss 9, p 1064 (2022)
This research was designed to identify thermodynamically and kinetically stable lipidic self-emulsifying formulations through simple energy dynamics in addition to highlighting and clarifying common ambiguities in the literature in this regard. Propo
Externí odkaz:
https://doaj.org/article/1a7cd89979d449f094b5dcba65946366
Autor:
Anum Munir Awan, Arshad Farid, Shefaat Ullah Shah, Dildar Khan, Fiza Ur Rehman, Muhammad Junaid Dar, Tayyaba Iftikhar, Shakira Ghazanfar, Charis M. Galanakis, Abdulhakeem S. Alamri, Syed Mohammed Basheeruddin Asdaq, Kifayat Ullah Shah
Publikováno v:
Pharmaceutics, Vol 14, Iss 6, p 1300 (2022)
The aim of this study was to improve the saturation solubility, dissolution profile and oral bioavailability of amiodarone hydrochloride (AMH), a highly lipophilic drug. Stabilizer (Pluronic F-127)-coated AMH nanocrystals (AMH-NCs) were developed by
Externí odkaz:
https://doaj.org/article/77b95f7f4c2a4517a0958063fe7e3604
Publikováno v:
Journal of Drug Delivery Science and Technology. 73:103429
Publikováno v:
Journal of biomedical materials research. Part B, Applied biomaterialsREFERENCES. 109(10)
Uncontrolled bleeding remains the leading cause of morbidity and mortality across the entire macrocosm. It refers to excessive loss of blood that occurs inside of body, due to unsuccessful platelet plug formation at the injury site. It is not only li
Autor:
Gul Majid Khan, Abhay R. Satoskar, Sidra Khalid, Kashif Iqbal, M. Junaid Dar, Saad Salman, Fiza Ur Rehman, Iffat Ullah
Publikováno v:
Nanomedicine: Nanotechnology, Biology and Medicine. 40:102490
The basic aim of the study was to develop and evaluate the triple drug loaded cationic nano-vesicles (cNVs), where miltefosine was used as a replacement of surfactant (apart from its anti-leishmanial role), in addition to meglumine antimoniate (MAM)
Autor:
Gul Shahnaz, Maryam Khatoon, Naseem Ullah, Fiza Ur Rehman, Asim Ur Rehman, Muhammad Farhan Sohail, Gul Majid Khan, Fakhar-Ud-Din, Umair Amin, Kifayat Ullah Shah
Publikováno v:
AAPS PharmSciTech. 20
Proniosomes offer excellent potential for improved drug delivery, through versatile routes, by overcoming the permeation barriers faced by several drugs. The study was aimed to develop a thiomer gel containing duloxetine proniosomes for the intranasa
Autor:
Rizwan Ahmed, Kehkashan Mazhar, Syeda Sohaila Naz, Kifayat Ullah Shah, Fiza Ur Rehman, Sara Qaisar, Annum Malik, Salman Khan, Adnan Khan
Publikováno v:
Materials Science and Engineering: C. 123:111940
Inflammatory cells orchestrate tumor niche for the proliferating neoplastic cells, leading to neoangiogenesis, lymphangiogenesis, tumor growth and metastasis. Emergence of severe side effects, multiple drug resistance and associated high cost has ren
Autor:
Amjad Khan, Kifayat Ullah Shah, Gul Majid Khan, Ikram Ullah Khan, Fiza Ur Rehman, Shefaat Ullah Shah
Publikováno v:
Expert Opinion on Drug Delivery. 14:1325-1340
Lipid-based drug delivery systems (LBDDS) are the most promising technique to formulate the poorly water soluble drugs. Nanotechnology strongly influences the therapeutic performance of hydrophobic drugs and has become an essential approach in drug d