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Startseite » News » Potential of solid dispersions to enhance solubility, bioavailability, and therapeutic efficacy of poorly water-soluble drugs: newer formulation techniques, current marketed scenario and patents

Potential of solid dispersions to enhance solubility, bioavailability, and therapeutic efficacy of poorly water-soluble drugs: newer formulation techniques, current marketed scenario and patents

22. November 2020
Solid-Dispersions

Solid-Dispersions

In the last few decades, solid dispersion (SD) technology had been studied as an approach to produce an amorphous carrier to enhance the solubility, dissolution rate, and bioavailability of poorly water-soluble drugs. The use of suitable carrier and methodology in the preparation of SDs play a significant role in the biological behavior of the SDs. SDs have been prepared using a variety of pharmaceutically acceptable polymers utilizing various novel technologies. In the recent years, much attention has been paid toward the use of novel carriers and methodologies in exploring novel types of SDs to enhance therapeutic efficacy and bioavailability. The use of novel carriers and methodologies would be very beneficial for formulation scientists to develop some SDs-based formulations for their commercial use and clinical applications. In the present review, current literature of novel methodologies for SD preparation to enhance the dissolution rate, solubility, therapeutic efficacy, and bioavailability of poorly water-soluble drugs has been summarized and analyzed. Further, the current status of SDs, patent status, and future prospects have also been discussed.

Download the full article here: Potential of solid dispersions to enhance solubility bioavailability and therapeutic efficacy of poorly water soluble drugs newer formulation

or continue reading here: Sultan Alshehri , Syed Sarim Imam , Afzal Hussain , Mohammad A. Altamimi , Nabil K. Alruwaili , Fahad Alotaibi , Abdullah Alanazi & Faiyaz Shakeel (2020) Potential of solid dispersions to enhance solubility, bioavailability, and therapeutic efficacy of poorly water-soluble drugs: newer formulation techniques, current marketed scenario and patents, Drug Delivery, 27:1, 1625-1643, DOI: 10.1080/10717544.2020.1846638

Some further insights of this article

DrugCarrierMethod
Nifedipine, efavirenzHydroxypropyl methylcellulose acetate succinateHot melt extrusion
Mefenamic acidEudragitVR EPOHot melt extrusion
Mefenamic acidKollidon® 12 PF and 17 PFHot melt extrusion
CarbamazepineSoluplus®Hot melt extrusion
PiperineEudragit® EPO, Kollidon® VA 64, Soluplus®Hot melt extrusion
LansoprazoleKollidon® 12 PF, Lutrol® F 68, MgOHot melt extrusion
AripiprazoleKollidon® 12 PF (PVP) and succinic acidHot-melt extrusion
HydrocortisonePolyethylene glycol 4000 (PEG 4000), Kolliphor® P 407Spray drying
ApigeninPluronic-F127Microwave irradiation
Mefenamic acid and flufenamic acidPluronic F127® (PL), Eudragit EPO® (EPO), polyethylene glycol 4000 (PEG 4000), Gelucire 50/13 (GLU)Microwave irradiation
Nifedipine, sulfamethoxazoleSoluplus®, PEG 6000Spray drying, lyophilization
Efavirenzhref="https://www.pharmaexcipients.com/product/soluplus/">Soluplus®Spray-drying
ApigeninPluronic F 127Spray drying
SirolimusEudragit® E HPMCSpray drying

 

Tags: excipientsformulation

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