Nanostructured lipid carriers (NLCs) as drug delivery platform: Advances in formulation and delivery strategies
2021 · Saudi Pharmaceutical Journal · 309 citations
https://doi.org/10.1016/j.jsps.2021.07.015
M
Mohammad M. Al‐Sanea
Jouf University(SA)
Claim or correct this author profile
Claim this profile or suggest corrections to the name, affiliation, bio, photo, or paper titles. Approved changes appear as verified CitedEvidence overlays.
137
Papers
3.0K
Citations
32
h-index
80
i10-index
Mohammad M. Al‐Sanea is an academic researcher from Jouf University. The author has contributed to research in topics: Synthesis and biological activity & Enzyme function and inhibition & Phytochemicals and Antioxidant Activities. The author has an h-index of 32, co-authored 117 publications.
ORCID: 0000-0002-9820-4022Papers by this author
worksSynthesis and biological evaluation of novel 3-(quinolin-4-ylamino)benzenesulfonamides as carbonic anhydrase isoforms I and II inhibitors
2019 · Journal of Enzyme Inhibition and Medicinal Chemistry · 26 citations
https://doi.org/10.1080/14756366.2019.1652282
Synthesis and biological evaluation of new pyrazol-4-ylpyrimidine derivatives as potential ROS1 kinase inhibitors
2014 · European Journal of Medicinal Chemistry · 16 citations
https://doi.org/10.1016/j.ejmech.2014.11.023
Inhibition of Bruton tyrosine kinase by acalabrutinib dampens lipopolysaccharide/galactosamine-induced hepatic damage
2020 · Biomedicine & Pharmacotherapy · 15 citations
https://doi.org/10.1016/j.biopha.2020.110736
Identification of non-classical hCA XII inhibitors using combination of computational approaches for drug design and discovery
2021 · Scientific Reports · 9 citations
https://doi.org/10.1038/s41598-021-94809-x
Simultaneous analysis of several antihypertensive drugs in different combinations: Application for determination of drug degradation products and process impurities
2021 · Microchemical Journal · 8 citations
https://doi.org/10.1016/j.microc.2021.106203
Research topics
topicsChat about Author
Papers
Chat
Click to start Chat