Pharmaceutical cocrystals, salts and multicomponent systems; intermolecular interactions and property based design

DJ Berry, JW Steed - Advanced drug delivery reviews, 2017 - Elsevier
As small molecule drugs become harder to develop and less cost effective for patient use,
efficient strategies for their property improvement become increasingly important to global …

Manufacturing of solid dispersions of poorly water soluble drugs by spray drying: formulation and process considerations

A Paudel, ZA Worku, J Meeus, S Guns… - International journal of …, 2013 - Elsevier
Spray drying is an efficient technology for solid dispersion manufacturing since it allows
extreme rapid solvent evaporation leading to fast transformation of an API-carrier solution to …

Solubility and dissolution enhancement strategies: current understanding and recent trends

S Jain, N Patel, S Lin - Drug development and industrial pharmacy, 2015 - Taylor & Francis
Identification of lead compounds with higher molecular weight and lower aqueous solubility
has become increasingly prevalent with the advent of high throughput screening. Poor …

Refining stability and dissolution rate of amorphous drug formulations

H Grohganz, PA Priemel, K Löbmann… - Expert opinion on …, 2014 - Taylor & Francis
Introduction: Poor aqueous solubility of active pharmaceutical ingredients (APIs) is one of
the main challenges in the development of new small molecular drugs. Additionally, the …

[HTML][HTML] Combining enabling formulation strategies to generate supersaturated solutions of delamanid: in situ salt formation during amorphous solid dispersion …

T Van Duong, HT Nguyen, LS Taylor - European Journal of Pharmaceutics …, 2022 - Elsevier
Poor solubility is a major challenge that can limit the oral bioavailability of many drugs,
including delamanid, a weakly basic nitro-dihydro-imidazooxazole derivative used to treat …

Amorphous salts solid dispersions of celecoxib: enhanced biopharmaceutical performance and physical stability

S Mukesh, P Joshi, AK Bansal… - Molecular …, 2021 - ACS Publications
Numerous amorphous solid dispersion (ASD) formulations of celecoxib (CEL) have been
attempted for enhancing the solubility, dissolution rate, and in vivo pharmacokinetics via …

The design and scale-up of spray dried particle delivery systems

A Al-Khattawi, A Bayly, A Phillips… - Expert opinion on drug …, 2018 - Taylor & Francis
Introduction: The rising demand for pharmaceutical particles with tailored physicochemical
properties has opened new markets for spray drying especially for solubility enhancement …

Formation and physicochemical properties of crystalline and amorphous salts with different stoichiometries formed between ciprofloxacin and succinic acid

KJ Paluch, T McCabe, H Muller-Bunz… - Molecular …, 2013 - ACS Publications
Multi-ionizable compounds, such as dicarboxylic acids, offer the possibility of forming salts of
drugs with multiple stoichiometries. Attempts to crystallize ciprofloxacin, a poorly water …

Preparation of an amorphous sodium furosemide salt improves solubility and dissolution rate and leads to a faster Tmax after oral dosing to rats

LH Nielsen, S Gordon, R Holm, A Selen… - European Journal of …, 2013 - Elsevier
Amorphous forms of furosemide sodium salt and furosemide free acid were prepared by
spray drying. For the preparation of the amorphous free acid, methanol was utilised as the …

Modulation of biopharmaceutical properties of acidic drugs using cationic counterions: A critical analysis of FDA-approved pharmaceutical salts

SS Bharate - International Journal of Pharmaceutics, 2021 - Elsevier
Salification has a successful track record in modulating the biopharmaceutical properties of
drugs. This is evident from the significant share (40%) of pharmaceutical salts in FDA …