[PDF][PDF] Triazine based dendrimer as solubility enhancers of ketoprofen: effect of concentration, pH and Generation
Methods: Triazine based dendrimer was synthesized up to generation 3 using divergent
method. Synthesized dendrimer generations were characterized by FT-IR, 1H-NMR and13C …
method. Synthesized dendrimer generations were characterized by FT-IR, 1H-NMR and13C …
[PDF][PDF] Enhanced solubility of non-steroidal anti-inflammatory drugs by hydroxyl terminated S-triazine based dendrimers
Methods: s-triazine based dendrimer was synthesized up to generation 3 by divergent
method. Synthesized dendrimer generations were characterized by IR, 1H-NMR, 13C-NMR …
method. Synthesized dendrimer generations were characterized by IR, 1H-NMR, 13C-NMR …
[PDF][PDF] Novel hydroxyl terminated dendrimers as potential drug carriers: Sustained release, hemolysis and cytotoxicity study
Objective: Potential of novel hydroxyl terminated dendrimer generations G1 (OH) 8, G2 (OH)
32 and G3 (OH) 128 as solubility enhancers of model drug ketoprofen was evaluated. G3 …
32 and G3 (OH) 128 as solubility enhancers of model drug ketoprofen was evaluated. G3 …
[HTML][HTML] Dendritic macromolecules as nano-scale drug carriers: Phase solubility, in vitro drug release, hemolysis and cytotoxicity study
Potential of nanoscale triazine based dendritic macromolecules G1, G2 and G3 as solubility
enhancers of drug was investigated. Effect of pH, concentration and generation of …
enhancers of drug was investigated. Effect of pH, concentration and generation of …
Polyamidoamine dendrimers used as solubility enhancers of ketoprofen
C Yiyun, X Tongwen, F Rongqiang - European Journal of Medicinal …, 2005 - Elsevier
Ketoprofen is a non-steroidal anti-inflammatory drug which is not freely soluble in water and
creates gastrointestinal problems. In the present study we investigated the potential of …
creates gastrointestinal problems. In the present study we investigated the potential of …
Solubility enhancement of aceclofenac using dendrimer
In the present study we investigated the effect of generation 3 (G3) PAMAM dendrimer on
the aqueous solubility of aceclofenac. The aqueous solubility of aceclofenac was measured …
the aqueous solubility of aceclofenac. The aqueous solubility of aceclofenac was measured …
[PDF][PDF] Polypropylene imine dendrimer mediated solubility enhancement: effect of pH and functional groups of hydrophobes
U Gupta, HB Agashe, NK Jain - J Pharm Pharm Sci, 2007 - academia.edu
Dendrimers today are known for their three dimensional, monodispersed, highly branched,
macromolecular nano-scopic architecture with number of reactive end groups. Dendrimers …
macromolecular nano-scopic architecture with number of reactive end groups. Dendrimers …
A comparative study on solubility improvement of tetracycline and dexamethasone by poly (propylene imine) and polyamidoamine dendrimers: An insight into …
F Najafi, M Salami‐Kalajahi… - … Research Part A, 2020 - Wiley Online Library
Many of new chemical discovered in pharmaceutical industry are hydrophobic compounds.
Various techniques have been used to overcome solubility problems of hydrophobic drugs …
Various techniques have been used to overcome solubility problems of hydrophobic drugs …
One platform comparison of solubilization potential of dendrimer with some solubilizing agents
S Jain, P Kesharwani, RK Tekade… - Drug development and …, 2015 - Taylor & Francis
Objective: To compare various solubilizing agents for their solubilizing propensity as well as
effect of pH, concentration and time on solubility of a highly hydrophobic drug. Materials and …
effect of pH, concentration and time on solubility of a highly hydrophobic drug. Materials and …
Synthesis of amphiphilic Janus dendrimer and its application in improvement of hydrophobic drugs solubility in aqueous media
F Najafi, M Salami-Kalajahi… - European Polymer …, 2020 - Elsevier
Classic dendrimers are not used in many specific applications such as simultaneous loading
of different drugs due to the existence of identical end groups. The possibility of designing …
of different drugs due to the existence of identical end groups. The possibility of designing …
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