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Published on: September 20, 2017
Cyclodextrin and phospholipid complexation in solubility and dissolution enhancement: a critical and meta-analysis
1H.N.B. Garhwal University Srinagar (Garhwal), Department of Pharmaceutical Sciences, Chauras Campus , Chauras, Srinagar (Garhwal), 246174 , India semaltyajay@yahoo.co.in.
Cyclodextrin (CD) and phospholipid (PL) complexation significantly enhance drug solubility and dissolution for poorly soluble drugs. These techniques improve drug absorption and bioavailability, offering valuable formulation strategies.
Area of Science:
- Pharmaceutical Sciences
- Drug Delivery
- Physical Chemistry
Background:
- Poor drug solubility and dissolution are critical challenges in pharmaceutical formulation and delivery.
- Cyclodextrin (CD) and phospholipid (PL) complexation are established methods to overcome these limitations.
Purpose of the Study:
- To review and critically analyze cyclodextrin (CD) and phospholipid (PL) complexation techniques for enhancing drug solubility and dissolution.
- To evaluate the potential of these complexation methods in improving drug absorption and bioavailability.
Main Methods:
- Discussion of various studies on CD and PL complexation for solubility enhancement.
- Critical review of physicochemical properties of CDs and PLs, drug eligibility, complexation thermodynamics, preparation methods, and characterization.
- Meta-analysis of selected studies for both complexation techniques.
Main Results:
- CD and PL complexation effectively improve the solubility and dissolution profiles of poorly water-soluble drugs.
- These complexation strategies demonstrate potential for enhancing drug absorption and overall bioavailability.
Conclusions:
- CD and PL complexation are highly effective for improving solubility, dissolution, and bioavailability of Biopharmaceutical Classification System (BCS) Class II and Class IV drugs.
- Selection of the appropriate complexation technique depends on drug eligibility, cost, stability, and demonstrated efficacy.
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