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1.
Pharm Dev Technol ; 29(2): 131-142, 2024 Feb.
Article in English | MEDLINE | ID: mdl-38235570

ABSTRACT

The aim of this work was to study the possibility to use SepitrapTM as a carrier for the formulation of amorphous solid dispersions by HME (hot melt extrusion) processing aiming solubility enhancement of poorly water-soluble drugs. SepitrapTM is a microencapsulated powder solubilizer designed to simplify the manufacture of drugs in oral solid forms, not yet tested for this purpose. The performance of SepitrapTM was evaluated in HME processing for amorphous solid dispersions of poorly-water soluble drugs with indomethacin as a model drug. The study was conducted using a twin-screw extruder, two compositions of SepitrapTM and different loads of indomethacin, demonstrating that SepitrapTM could represent a new range of carriers for amorphous solid dispersions for HME processing, reducing necessary downstream steps such as grinding.


Subject(s)
Chemistry, Pharmaceutical , Indomethacin , Drug Compounding , Hot Melt Extrusion Technology , Solubility , Water , Hot Temperature , Drug Carriers
2.
Eur J Pharm Biopharm ; 142: 300-306, 2019 Sep.
Article in English | MEDLINE | ID: mdl-31247317

ABSTRACT

Amorphous solid dispersions (ASDs) are found to be a well-established strategy for overcoming limited aqueous solubility and poor oral bioavailability of active pharmaceutical ingredients (APIs). One of the main parameters affecting ASDs physical stability is the API solubility in the carrier, because this value determines the maximal API load without a risk of phase separation and recrystallization. Phase-diagrams can be experimentally obtained by following the recrystallization of the API from a supersaturated homogeneous API-polymer solid solution, commonly produced by processes as solvent casting or comilling, which are very time-consuming (hours). The work deals with the construction of a temperature-composition EFV-Soluplus® phase diagram, from a thermal study of recrystallization of a supersaturated solid solution (85 wt% in EFV) generated by spray drying. This supersaturated solution is kept at a given annealing temperature to reach the equilibrium state and the amount that still remains dispersed in the polymer carrier at this equilibrium temperature is determined by means of the new glass transition temperature of the binary mixture. From our knowledge, this is the first study employing a fast process (spray drying) to prepare a supersaturated solid solution of an API in a polymer aiming to determine a temperature-composition phase diagram. The EFV solubility in Soluplus ranges from 20 wt% at 25 °C to 30 wt% at 40 °C. It can be a very useful preformulation tool for researchers studying amorphous solid dispersions of Efavirenz in Soluplus, to assist for predicting the stability of EFV-Soluplus ASDs at different EFV loadings and under different thermal conditions.


Subject(s)
Benzoxazines/chemistry , Polyethylene Glycols/chemistry , Polymers/chemistry , Polyvinyls/chemistry , Alkynes , Calorimetry, Differential Scanning/methods , Chemistry, Pharmaceutical/methods , Crystallization , Cyclopropanes , Desiccation/methods , Drug Carriers/chemistry , Drug Compounding/methods , Drug Stability , Solubility/drug effects , Solvents/chemistry , Transition Temperature
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