Zobrazeno 1 - 10
of 60
pro vyhledávání: '"Omaima N, El Gazayerly"'
Publikováno v:
Journal of Research in Pharmacy. 27:30-42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e1b295ee4ef57272867e2cd5b7d7861
https://doi.org/10.29228/jrp.285
https://doi.org/10.29228/jrp.285
Autor:
Mohamed Ali, Amira Abdel Motaal, Mohammed A. Ahmed, Abdulrhman Alsayari, Omaima N. El-Gazayerly
Publikováno v:
Drug Delivery, Vol 25, Iss 1, Pp 417-425 (2018)
The active compounds present in Hypericum perforatum L. (Hypericaceae) include hyperforin, hypericins and flavonoids, which are assumed to be responsible for the activity of the extract in the treatment of wounds and scars. The present study aimed to
Externí odkaz:
https://doaj.org/article/b75903f7f6e9440e924b1e00b24eac42
Publikováno v:
Drug Delivery, Vol 25, Iss 1, Pp 1161-1174 (2018)
Gabapentin (GBP), an antiepileptic and anti-neuropathic agent, suffers from short half-life (5–7 h), has narrow absorption window, and is absorbed via carrier-mediated mechanism resulting in frequent dosing, poor compliance, and poor bioavailabilit
Externí odkaz:
https://doaj.org/article/921b536415de41538017a608dc60df8f
Publikováno v:
Drug Delivery, Vol 25, Iss 1, Pp 1448-1460 (2018)
Controlled-release multiparticulate systems of hydrophilic drugs usually suffer from poor encapsulation and rapid-release rate. In the present study, ultra-high loaded controlled release polymeric beads containing verapamil hydrochloride (VP) as hydr
Externí odkaz:
https://doaj.org/article/f88d0929607b44468d177eaed4eb829e
Publikováno v:
Future Journal of Pharmaceutical Sciences, Vol 3, Iss 2, Pp 90-94 (2017)
Olmesartan medoxomil (OLM) is highly lipophilic in nature (log p = 4.31) which attributes to its low aqueous solubility contributing to its low bioavailability 25.6%. OLM was loaded into mixed micelles carriers in a trial to enhance its solubility, t
Externí odkaz:
https://doaj.org/article/05c5adbbcb904773b638e5b0bec42067
Publikováno v:
AAPS PharmSciTech. 24
The current study is regarding the development and characterization of Darifenacin-loaded self-assembled liquid crystal cubic nanoparticles (LCCN). An anhydrous approach was used for the preparation of these cubic nanoparticles using a hydrotropic ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5a95d58a485b8d81f6850e62fd51759
https://doi.org/10.1208/s12249-023-02575-y
https://doi.org/10.1208/s12249-023-02575-y
Publikováno v:
International Journal of Applied Pharmaceutics. :189-197
Objective: To design topical Quercetin (Qc)-loaded transfersomes (TFs) for wound treatment. Methods: Qc-loaded TFs were prepared by thin-film hydration technique using 2241full factorial design and the optimum formula was selected. In vivo skin, depo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec9f0ad59ef574cc4964d6e719348683
https://doi.org/10.22159/ijap.2021v13i5.41345
https://doi.org/10.22159/ijap.2021v13i5.41345
Autor:
Aya A. Mabrouk, Nesrine S. El-Mezayen, Mina I. Tadros, Omaima N. El-Gazayerly, Wessam M. El-Refaie
Publikováno v:
European journal of pharmaceutics and biopharmaceutics : official journal of Arbeitsgemeinschaft fur Pharmazeutische Verfahrenstechnik e.V.
Oral squamous-cell carcinoma (OSCC) is a widespread health problem. Myeloid-derived suppressor cells (MDSCs) are major tumor microenvironment (TME) population that govern many carcinogenesis aspects by establishing immunosuppressive milieu favoring t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f14470bf864e43229ea5e1d4c0294ee
https://pubmed.ncbi.nlm.nih.gov/36513316
https://pubmed.ncbi.nlm.nih.gov/36513316
Publikováno v:
Pharmaceutics, Vol 11, Iss 6, p 257 (2019)
In this work, ultrahigh drug-loaded chitosan (Ch)/K-carrageenan (Kc) polyelectrolyte complex (PEC) beads were formed in situ by cross-linking in a glutaraldehyde-saturated atmosphere and were prepared on superhydrophobic substrates fabricated by spra
Externí odkaz:
https://doaj.org/article/1a21a2d5024044209bd959d97e83e1f6
Publikováno v:
International Journal of Pharmaceutics. 636:122852
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d070a2e9628d9d5d06e49d31277df6c0
https://doi.org/10.1016/j.ijpharm.2023.122852
https://doi.org/10.1016/j.ijpharm.2023.122852