[PDF][PDF] Brief overview of various approaches to enhance drug solubility
… Poor solubility limits drug delivery and formulation development. Various techniques have
been developed to enhance solubility of poorly soluble drugs. Pharmaceuticals falling under …
been developed to enhance solubility of poorly soluble drugs. Pharmaceuticals falling under …
Solubility enhancement and application of cyclodextrins in local drug delivery
DH Kim, SE Lee, YC Pyo, P Tran, JS Park - Journal of Pharmaceutical …, 2020 - Springer
… for drugs with poor aqueous solubility and low bioavailability. Because CDs can act as drug
… conjugate with many drugs, they have been applied in many drug delivery systems and can …
… conjugate with many drugs, they have been applied in many drug delivery systems and can …
Self-Emulsifying Drug Delivery System: An Approach to Enhance Solubility.
… drug delivery systems (SEDDSs) have gained exposure for their ability to increase solubility
and bioavailability of poorly soluble drugs. … of the sparingly soluble drugs by rapid self-…
and bioavailability of poorly soluble drugs. … of the sparingly soluble drugs by rapid self-…
Self emulsifying drug delivery system for enhanced solubility and dissolution of glipizide
AG Agrawal, A Kumar, PS Gide - Colloids and Surfaces B: Biointerfaces, 2015 - Elsevier
… drug delivery systems (SEDDS) of glipizide and to convert it into solid SEDDS (S-SEDDS)
using Syloid ® 244 FP as adsorbent. Solubility … -SEDDS compared with pure drug. The results …
using Syloid ® 244 FP as adsorbent. Solubility … -SEDDS compared with pure drug. The results …
Novel self-nanoemulsifying drug delivery system for enhanced solubility and dissolution of lutein
JH Yoo, S Shanmugam, P Thapa, ES Lee… - Archives of pharmacal …, 2010 - Springer
… drug delivery system (SNEDDS) containing oil (Phosal 53 MCT), surfactant (Labrasol),
and cosurfactant (Transcutol-HP or Lutrol-E400) was prepared to enhance solubility and …
and cosurfactant (Transcutol-HP or Lutrol-E400) was prepared to enhance solubility and …
Solubility enhancers for oral drug delivery: can chemical structure manipulation be avoided?
CK Kim, JS Park - American Journal of Drug Delivery, 2004 - Springer
… solubility properties.[2] The aim of this article is to review ways in which the solubility of these
highly lipophilic drugs can be enhanced, … that do not alter the chemical structure of the drug. …
highly lipophilic drugs can be enhanced, … that do not alter the chemical structure of the drug. …
[HTML][HTML] Design, optimization and evaluation of glipizide solid self-nanoemulsifying drug delivery for enhanced solubility and dissolution
RN Dash, H Mohammed, T Humaira… - Saudi Pharmaceutical …, 2015 - Elsevier
… drug-delivery system (solid SNEDDS) has been explored to improve the solubility and …
area for drug solubilization leading to an enhanced solubility and dissolution of glipizide. …
area for drug solubilization leading to an enhanced solubility and dissolution of glipizide. …
Drug solubility: importance and enhancement techniques
KT Savjani, AK Gajjar, JK Savjani - … Scholarly Research Notices, 2012 - Wiley Online Library
… The improvement of drug solubility thereby its oral bio-… of drug development process
especially for oral-drug delivery … literature to enhance the solubility of poorly water-soluble drugs. …
especially for oral-drug delivery … literature to enhance the solubility of poorly water-soluble drugs. …
Ultra fine super self-nanoemulsifying drug delivery system (SNEDDS) enhanced solubility and dissolution of indomethacin
… solubility studies showed around 4573 fold enhancement in solubility in F1 formulation
compared to its aqueous solubility… drug delivery of IND in order to enhance its solubility as well as …
compared to its aqueous solubility… drug delivery of IND in order to enhance its solubility as well as …
Application of dendrimer–drug complexation in the enhancement of drug solubility and bioavailability
NK Jain, U Gupta - Expert opinion on drug metabolism & toxicology, 2008 - Taylor & Francis
… In addition dendrimers can be surface engineered to release the drug at desired site, that
is, as targeted drug delivery. This property along with the solubilisation behaviour could …
is, as targeted drug delivery. This property along with the solubilisation behaviour could …
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