Results 11 to 20 of about 4,959 (213)
NANOSUSPENSION: AN OVERVIEW [PDF]
International Journal of Current Pharmaceutical Research, 2017 Nanosuspensions are important carriers to develop novel drug formulations. Nanosuspensions have emerged as a promising strategy for the efficient delivery of hydrophobic drugs because of their versatile features and unique advantages. Nanosuspension technology solved the problem of drugs which are poorly aqueous soluble and less bioavailability ...
Smita S. Aher +2 more
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ANTIBIOTICS NANOSUSPENSION: A REVIEW [PDF]
Journal of Drug Delivery and Therapeutics, 2017 Nanosuspensions are colloidal dispersions and biphasic system consisting of drug particles dispersed in an aqueous vehicle in which the diameter of the suspended particle is less than 1μm in size. Many drugs including antibiotics are having poor solubility. Nanosuspensions have proven to be a better alternative over other approaches currently available
Merin Mathew +3 more
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Journal of Drug Delivery and Therapeutics, 2013 Nanotechnology has emerged as a tremendous field in the medicine. Nano refers to particles size range of 1-1000nm. Nanosuspensions are part of nanotechnology. Nanosuspensions contain submicron colloidal dispersion of pharmaceutical active ingredient particles in a liquid phase stabilized by surfactants.
Akanksha Chandra +3 more
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Nanosuspension: An approach to enhance solubility of drugs
Journal of Advanced Pharmaceutical Technology & Research, 2011 One of the major problems associated with poorly soluble drugs is very low bioavailability. The problem is even more complex for drugs like itraconazole, simvastatin, and carbamazepine which are poorly soluble in both aqueous and nonaqueous media ...
Vishal R Patel, Y K Agrawal
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Preparation, characterization and pharmacokinetics of cyadox nanosuspension
Scientific Reports, 2017 An increase in number of newly developed synthetic drugs displays bioavailability constraints because of poor water solubility. Nanosuspensions formulation may help to overwhelm these problems by increasing dissolution velocity and saturation solubility.
Adeel Sattar +8 more
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An Overview of Recent Patents on Nanosuspension
Recent Patents on Drug Delivery & Formulation, 2014 Pharmaceutical scientists involved in drug discovery and drug development are facing serious problems with newer poorly water soluble drugs with respect to their dissolution and bioavailability. Reducing the particle size of active pharmaceutical ingredient has been an efficient and reliable method for improving the bioavailability of insoluble drugs ...
Modh, Nirav +4 more
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NANOSUSPENSION TECHNOLOGY: A REVIEW
, 2021 Solubility is the crucial factor for drug effectiveness, independence of the route of administration. Large proportions of newly discovered drugs are water insoluble, and therefore poorly bioavailable contributing to deserted development effort. These so‐called 'Brickellia' candidates can now be delivered by formulating them into Nanosuspension ...
T. Pavani Priya, K. Manasa, Ch. Greeshmika1, B. Hemalatha, K. Padmalatha
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Effects of oridonin nanosuspension on cell proliferation and apoptosis of human prostatic carcinoma PC-3 cell line [PDF]
International Journal of Nanomedicine, 2010 Zhen Zhang, Xiumei Zhang, Wei Xue, Yuna YangYang, Derong Xu, Yunxue Zhao, Haiyan LouSchool of Medicine, Shandong University, Jinan, Republic of ChinaAbstract: This study aims to investigate the inhibitory effects of oridonin nanosuspension on human ...
Zhen Zhang, Xiumei Zhang, Wei Xue, et al
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International Journal of Nanomedicine, 2016 Thawatchai Phaechamud,1 Sarun Tuntarawongsa2 1Department of Pharmaceutical Technology, 2Pharmaceutical Intelligence Unit Prachote Plengwittaya, Faculty of Pharmacy, Silpakorn University, Nakhon Pathom, Thailand Abstract: Eutectic solvent can solubilize
Phaechamud T, Tuntarawongsa S
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Enhancement of oral bioavailability of quercetin by metabolic inhibitory nanosuspensions compared to conventional nanosuspensions [PDF]
Drug Delivery, 2021 Quercetin-loaded nanosuspensions (Que-NSps) added metabolic inhibitors were evaluated as drug delivery system to promote the oral bioavailability of quercetin. Que-NSps were prepared respectively using d-alpha tocopherol acid polyethylene glycol succinate (TPGS) or Soybean Lecithin (SPC) as stabilizer. On the basis, Piperine (Pip) or sodium oleate (SO)
Haowen Li +5 more
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