7 results match your criteria: "S.M.B.T. College of Pharmacy[Affiliation]"
Zhongguo Ying Yong Sheng Li Xue Za Zhi
December 2023
Department of Pharmaceutical Chemistry, S.M.B.T. College of Pharmacy, Affiliated to Savitribai Phule Pune University, Dhamangaon, Nashik, M.S. India-422403.
Silver nanoclusters (AgNCs) have emerged as versatile nanomaterials with immense potential in theranostic applications, combining therapeutic and diagnostic functions in a single platform. This review provides a comprehensive overview of recent advancements in the synthesis, characterization, and utilization of AgNCs for theranostics. The synthesis of AgNCs has witnessed significant progress, with numerous strategies such as chemical reduction, green synthesis, and templated approaches being employed to control size, shape, and stability.
View Article and Find Full Text PDFRecent Adv Drug Deliv Formul
April 2023
Department of Pharmaceutics, S.M.B.T. College of Pharmacy, Dhamangaon, Nashik, India.
The pulmonary drug delivery system is a minimally invasive method of administering drugs with systemic and localised activity. Since 4000 BC, inhalation therapy has been known to the Indians. The most effective and suitable pulmonary drug delivery methods have been used for controlling diseases like asthma, chronic obstructive pulmonary disorder (COPD), TB(Tuberculosis), lung cancer, cystic fibrosis, and pulmonary hypertension.
View Article and Find Full Text PDFBioorg Chem
July 2022
Department of Pharmacognosy, S.M.B.T. College of Pharmacy, Affiliated to Savitribai Phule Pune University, Dhamangaon, Nashik, M.S. 422403, India.
Thiosemicarbazides (TSCs), dithiocarbamates (DTCs) and their molecular conjugates are promising drug targets. However, hybrids of DTCs with TSCs themselves are rarely investigated. Thus, studies were initiated to synthesize novel system derived from TSC-DTCs to examine their pharmacological applications.
View Article and Find Full Text PDFNat Prod Res
December 2022
Department of Pharmacognosy, S.M.B.T. College of Pharmacy, Nashik, India.
The present study is aimed to evaluate thrombolytic activity and antioxidant activity of L. Chemical characterization of bioactive extract was determined by using GC-MS analysis. The thrombolytic potential was performed by the clot lysis method.
View Article and Find Full Text PDFTurk J Chem
September 2021
Department of Pharmaceutical Chemistry, S.M.B.T. College of Pharmacy, Dist-Nashik, India.
A novel four component modified Biginelli reaction for the synthesis of C-2 functionalized dihydropyrimidines has been established. The approach uses assembly of less explored acetyl acetone with aromatic aldehyde, thiourea, and dimethyl sulphate to construct a novel 5-acetyl 2-methylthio dihydropyrimidine system, which works as an efficient well-designed intermediate for generating C-2 modified Biginelli libraries with nitrogen nucleophiles. Phenyl hydrazine, semicarbazide, and aryl semicarbazides are successfully used as N-nucleophiles to generate C-2 functionalized dihydropyrimidine derivatives, which fulfil the demands of active pharmacophore.
View Article and Find Full Text PDFTurk J Pharm Sci
August 2018
A.R.A. College of Pharmacy, Dhule, India.
Objectives: The present study aims to assess the antidepressant activity of extracts in mice and phytochemical analysis of the active extract by GC-MS.
Materials And Methods: After oral administration of extracts, tail suspension test (TST), force swim tests (FST), and open field tests (OFT) were performed to assess the antidepressant activity. GC-MS analysis of methanol extract of was performed to ascertain the chemical constituents in the bioactive extract.
Pak J Pharm Sci
March 2017
Department of Pharmaceutical Chemistry, A. R. A. College of Pharmacy, Nagaon, Dhule, Maharashtra, India.
The title compound, 3-(4-chlorophenyl)-4-formyl-[1, 2, 3] oxadiazol-3-ium-5-olate 5 was synthesized under ultrasonication by formylation of 3-(4-chlorophenyl)-[1, 2, 3] oxadiazol-3-ium-5-olate 4 and characterized by spectral studies. The ultrasonic method of synthesis was found to be simple, ecofriendly, economical, reduces reaction time and gave good yield when compared with traditional methods of synthesis. Anticancer activity of the compounds were tested against 60 human tumor cell lines and compared with standard drug vincristine sulphate.
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