scholarly journals Practical Approach to Modeling the Impact of Amorphous Drug Nanoparticles on the Oral Absorption of Poorly Soluble Drugs

2019 ◽  
Vol 17 (1) ◽  
pp. 180-189 ◽  
Author(s):  
Aaron M. Stewart ◽  
Michael E. Grass
Author(s):  
Risa Aihara ◽  
Roman Messerschmid ◽  
Masashi Mizoguchi ◽  
Koichi Wada ◽  
Keiko Minami ◽  
...  

2010 ◽  
Vol 99 (3) ◽  
pp. 1336-1345 ◽  
Author(s):  
Koji Yano ◽  
Yoshie Masaoka ◽  
Makoto Kataoka ◽  
Shinji Sakuma ◽  
Shinji Yamashita

2016 ◽  
Vol 95 ◽  
pp. 138-144 ◽  
Author(s):  
Kateřina Punčochová ◽  
Marie Prajzlerová ◽  
Josef Beránek ◽  
František Štěpánek

2021 ◽  
Vol 22 (9) ◽  
pp. 4338
Author(s):  
Rita Caparica ◽  
Ana Júlio ◽  
Filipe Fernandes ◽  
Maria Eduarda M. Araújo ◽  
João Guilherme Costa ◽  
...  

Numerous studies are continuously being carried out in pursuit of formulations with higher performance. Problems such as poor drug solubility, which hinders drug incorporation into delivery systems and bioavailability, or limitations concerning the stability and performance of the formulations may cause difficulties, since solving all these drawbacks at once is a huge challenge. Ionic liquids (ILs), due to their tunable nature, may hypothetically be synthesized for a particular application. Therefore, predicting the impact of a particular combination of ions within an IL in drug delivery could be a useful strategy. Eight ILs, two choline amino acid ILs, two imidazole halogenated ILs, and four imidazole amino acid ILs, were prepared. Their applicability at non-toxic concentrations, for improving solubility and the incorporation of the poorly soluble, ferulic, caffeic, and p-coumaric acids, as well as rutin, into topical emulsions, was assessed. Next, the impact of the ILs on the performance of the formulations was investigated. Our study showed that choosing the appropriate IL leads to a clear upgrade of a topical emulsion, by optimizing multiple features of its performance, such as improving the delivery of poorly soluble drugs, altering the viscosity, which may lead to better sensorial features, and increasing the stability over time.


2012 ◽  
Vol 101 (1) ◽  
pp. 214-222 ◽  
Author(s):  
Shunsuke Ozaki ◽  
Takuma Minamisono ◽  
Taro Yamashita ◽  
Takashi Kato ◽  
Ikuo Kushida

2016 ◽  
Vol 34 (1) ◽  
pp. 208-216 ◽  
Author(s):  
Kohsaku Kawakami ◽  
Aoi Miyazaki ◽  
Mayuko Fukushima ◽  
Keiko Sato ◽  
Yuko Yamamura ◽  
...  

2017 ◽  
Vol 5 (04) ◽  
pp. 17-23
Author(s):  
Katta Manogna ◽  
P. Nagaveni ◽  
K. Thyagaraju

Most of the newly invented chemical drug moieties are poorly water soluble. According to BCS classification, class II and IV drugs are considered as poorly water soluble. So enhancement of oral absorption and bioavailability of solid dosage forms remains a challenge to formulation scientists due to their solubility criteria. Therefore many techniques are being explored to enhance the solubility of poor soluble drugs. Solid dispersion is one of the most important method for enhance the solubility (dissolution rate) and hence oral bioavailability of poorly soluble drugs. In solid dispersion the particle size of drug is reduced or a crystalline pure drug is converted into amorphous form and hence the solubility is increased. Polymer incorporating in solid dispersion technology is usually hydrophilic in nature and also showing compatibility with the drug to enhance the drug solubility. This review mainly discus about solid dispersion, preparation methods, and finally characterization.


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