Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Maria Abdul Ghafoor Raja"'
Publikováno v:
Asian Journal of Pharmaceutical Sciences, Vol 14, Iss 5, Pp 497-510 (2019)
Upon the discovery of RNA interference (RNAi), canonical small interfering RNA (siRNA) has been recognized to trigger sequence-specific gene silencing. Despite the benefits of siRNAs as potential new drugs, there are obstacles still to be overcome, i
Externí odkaz:
https://doaj.org/article/5a069e9d8d5341639ba2d4c884d73492
Autor:
Muhammad Zaman, Rabia Imtiaz Bajwa, Omer Salman Qureshi, Atta Ur Rehman, Sadaf Saeed, Muhammad Wahab Amjad, Maria Abdul Ghafoor Raja, Muhammad Ajaz Hussain
Publikováno v:
Frontiers in Pharmacology, Vol 12 (2021)
Background: Nature has always been considered as the primary source of pharmaceutical ingredients. A variety of hemicelluloses, as well as their modified forms, have been under investigation. Herein, a study was designed to explore the biocompatibili
Externí odkaz:
https://doaj.org/article/f9a33506a37d4ba5a287c4c46b0780f1
Publikováno v:
PLoS ONE, Vol 10, Iss 6, p e0128963 (2015)
Chitosan (CS) nanoparticles have been extensively studied for siRNA delivery; however, their stability and efficacy are highly dependent on the types of cross-linker used. To address this issue, three common cross-linkers; tripolyphosphate (TPP), dex
Externí odkaz:
https://doaj.org/article/4e8e8ef9ca594f85ba70c3d3b0e1256e
Publikováno v:
International Journal of Biomaterials, Vol 2013 (2013)
Chitosan nanoparticles (CS NPs) exhibit good physicochemical properties as drug delivery systems. The aim of this study is to determine the modulation of preparative parameters on the physical characteristics and colloidal stability of CS NPs. CS NPs
Externí odkaz:
https://doaj.org/article/50ff6618c1c04cb693ff44355d7810c5
Autor:
Mohammad M. Al-Sanea, Syed Nasir Abbas Bukhari, Muhammad Ajaz Hussain, Muhammad Masood Ahmad, Khalid Saad Alharbi, Mohamed A. Abdelgawad, Muhammad Amjad, Waqas Ahmad, Nasser Hadal Alotaibi, Maria Abdul Ghafoor Raja
Publikováno v:
Medicinal Chemistry. 17:956-962
Background: Ligustrazine and chalcones have been reported previously for various biological activities including anticancer effects. Objectives: Based on the multitargeted biological activities approach of ligustrazine-based chalcones, in the current
Publikováno v:
Tropical Journal of Pharmaceutical Research. 18:1347-1352
Purpose: To assess the prevalence of handwritten prescription errors in Rafha Central Hospital in Saudi Arabia, and to determine the most predominant type of prescription error. Methods: A cross-sectional study was carried out on randomly selected sa
Publikováno v:
Journal of Pharmaceutical Research International. :18-24
Every year millions of new cases of various types of cancers are diagnosed, leading to an alarming rate of fatalities. Mitoxantrone is an anthracenedione antineoplastic agent which is used in the treatment of various types of cancer, mostly acute mye
Publikováno v:
Journal of Pharmaceutical Research International. :33-39
Nanotechnology facilitated drug delivery has been used to enhance the drug bioavailability, efficacy, reduce toxicity and improve patient compliance aiming to targetthe cells and tissues to produce anticipated pharmacological action. The aim of the p
Autor:
Muhammad Zaman, Umer Farooq, Muhammad Amjad, Shahid Shah, Syed Farhan Haider Rizvi, Asma Iqbal, Maria Abdul Ghafoor Raja, Sharjeel Adnan, Mian Waqar Mustafa, Ghulam Abbas
Publikováno v:
International Journal of Nanomedicine. 15:5603-5612
Introduction Organ transplantation is a critically important procedure, which requires immune modulation by using immunosuppressants. Development of nanoparticles is an emerging and beneficial engineering process to increase the dissolution rate of p
Autor:
Muhammad Amjad, Ghulam Abbas, Shahid Shah, Maria Abdul Ghafoor Raja, Omeira Iqbal, Muhammad Hanif, Mehran Ashfaq, Muhammad Zaman, Akhtar Rasul, Hafeez Ullah Khan
Publikováno v:
International Journal of Nanomedicine. 15:4847-4858
Background Bisphosphonates have very low bioavailability and cause irritation of the esophagus and stomach. This study was planned to improve the oral bioavailability of ibandronate through the formation of a raft in the stomach. Bisphosphonate-induc