Physicochemical analysis in the evaluation of reconstituted dry emulsion tablets

被引:4
|
作者
Niczinger, Noemi Anna [1 ]
Kallai-Szabo, Barnabas [1 ]
Lengyel, Milena [1 ]
Gordon, Peter [2 ]
Klebovich, Imre [1 ]
Antal, Istvan [1 ]
机构
[1] Semmelweis Univ, Dept Pharmaceut, 7 Hogyes Endre Str, H-1092 Budapest, Hungary
[2] Budapest Univ Technol & Econ, Dept Elect Technol, 18 Egry J Str, H-1111 Budapest, Hungary
关键词
Olive oil; Required HLB; Contact angle; Laser diffraction; Turbidimetry; Scanning microscopy; DRUG-DELIVERY SYSTEMS; POORLY SOLUBLE DRUGS; REQUIRED HLB; IN-VITRO; OIL;
D O I
10.1016/j.jpba.2016.11.031
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The aim of this study was to characterize the formation of emulsions by droplet size analysis and turbidimetry during reconstitution from a solid dosage form, namely from dry emulsion systems, which carry an oil phase for poorly soluble active ingredients. For the dry emulsion systems tablets were prepared either from oil-in-water systems using a freeze-drying process or through direct compression containing the same oil and excipients. The ratios of oil to emulgents and oil to xanthan gum were equal in both methods. In the preparation methods applied, mannitol, erythritol and lactose were used as excipients and mannitol was found to be the most effective excipient based on droplet size reconstitution, turbidimetry and physical properties. Quality control involved testing the physical properties of tablets and characterizing the reconstituted emulsions. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:86 / 93
页数:8
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