Structure-property relationship in the evaluation of xanthan gum functionality for oral suspensions and tablets

被引:2
作者
Yang, Qiuxia [1 ]
Li, Ying [2 ]
Cao, Zhen [1 ,3 ]
Miao, Jiaying [1 ]
Feng, Jiaqi [1 ]
Xi, Quan [1 ,4 ]
Lu, Weigen [1 ,4 ]
机构
[1] China State Inst Pharmaceut Ind Co Ltd, Shanghai Inst Pharmaceut Ind Co Ltd, Shanghai 201203, Peoples R China
[2] Tongji Univ, Shanghai Skin Dis Hosp, Sch Med, Shanghai 200443, Peoples R China
[3] China Pharmaceut Univ, Key Lab Drug Qual Control & Pharmacovigilance, Minist Educ, Nanjing 210009, Peoples R China
[4] China State Inst Pharmaceut Ind Co Ltd, 285, Gebaini Rd, Shanghai 201203, Peoples R China
关键词
Xanthan gum; Structure-property relationship; Functionality; Oral suspensions; Matrix tablets; DRUG-RELEASE; RHEOLOGICAL PROPERTIES; EXCIPIENT VARIABILITY; MATRIX TABLETS; BEHAVIOR; PYRUVATE; GEL; RECOVERY; DELIVERY; STRAINS;
D O I
10.1016/j.ijbiomac.2022.12.081
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The functional properties of xanthan gum (XG) in pharmaceutical preparations depend on its rheological properties, which inevitably rely on its molecular structure. Hence, this work investigated the relationship be-tween the molecular structure of XG and its rheological properties and functional characteristics, and revealed the structural factors influencing the XG functionalities in oral suspensions and matrix tablets. Primarily, the molecular structures of four commercial XG products were characterized by infrared spectroscopy, differential scanning calorimetry and measuring the monosaccharide composition, average molecular weight, and pyruvate and acetyl contents. Furthermore, the flow behavior and viscoelasticity of XG solutions, the viscoelasticity of XG hydrogels, and XG combinations (XGC, aqueous solution containing XG, liquid glucose, and glycerin) were investigated. Finally, the dissolution time of XGC and the swelling and erosion properties of the XG matrix were studied to evaluate XG functionality in oral suspensions and matrix tablets, respectively. Results showed that the polydispersity of molecular weight and the pyruvate content affected the functionality and performance of XG in suspension and tablet forms. The higher polydispersity and pyruvate content of XG improved the hydrogel strength, which led to a longer dissolution time of XGC and a higher swelling extent of the XG matrix but a slower erosion rate.
引用
收藏
页码:525 / 534
页数:10
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