Is rat a good model for assessment of particulate-based taste-masked formulations?

被引:4
作者
Ali, Joseph [1 ]
Chiang, Manting [2 ]
Lee, Jong Bong [2 ]
Voronin, Gregory O. [2 ]
Bennett, Joanne [3 ]
Cram, Anne [3 ]
Kagan, Leonid [2 ]
Garnett, Martin C. [1 ]
Roberts, Clive J. [1 ]
Gershkovich, Pavel [1 ]
机构
[1] Univ Nottingham, Sch Pharm, Univ Pk, Nottingham NG7 2RD, England
[2] Rutgers State Univ, Ernest Mario Sch Pharm, Dept Pharmaceut, Piscataway, NJ 08854 USA
[3] Pfizer Ltd, Discovery Pk,Ramsgate Rd, Sandwich CT13 9ND, Kent, England
基金
英国工程与自然科学研究理事会;
关键词
Rat saliva; Oral cavity; Dissolution; Particulate-based taste-masked formulation; DISSOLUTION MEDIUM; VIVO CORRELATIONS; SURFACE-TENSION; GASTRIC-JUICE; BITTER TASTE; HUMAN SALIVA; MEDICINES; ACCEPTABILITY; SOLUBILITY; CAPACITY;
D O I
10.1016/j.ejpb.2019.11.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Recently there has been an increased interest to develop specialised dosage forms that are better suited to specific patient populations, such as paediatrics and geriatrics. In these patient populations the acceptability of the oral dosage form can be paramount to the products success. However, many Active Pharmaceutical Ingredients (APIs) are known to cause an aversive taste response. One way to increase the acceptability and to enhance the palatability of the formulation is to design coated taste-masked particulate-based dosage forms. The masking of poorly tasting drugs with physical barriers such as polymer coatings can be utilised to prevent the release of drug within the oral cavity, thus preventing a taste response. However, currently, there are few assessment tools and models available to test the efficiency of these particulate-based taste-masked formulations. The rat brief access taste aversion model has been shown to be useful in assessment of taste for liquid dosage forms. However, the applicability of the rat model for particulate-based taste masked formulations is yet to be assessed. It is not understood whether dissolution, solubility and thus exposure of the drug to taste receptors would be the same in rat and human. Therefore, rat saliva must be compared to human saliva to determine the likelihood that drug release would be similar within the oral cavity for both species. In this study rat saliva was characterised for parameters known to be important for drug dissolution, such as pH, buffer capacity, surface tension, and viscosity. Subsequently dissolution of model bitter tasting compounds, sildenafil citrate and efavirenz, in rat saliva was compared to dissolution in human saliva. For all parameters characterised and for the dissolution of both drugs in rat saliva, a substantial difference was observed when compared to human saliva. This discrepancy in saliva parameters and dissolution of model drugs suggests that preclinical taste evaluation of particulate-based taste-masked formulations suggests rat is not a good model for predicting taste of solid dosage forms or undissolved drug where dissolution is required. Alternative preclinical in vivo models in other species, or improved biorelevant in vitro models should be considered instead.
引用
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页码:1 / 9
页数:9
相关论文
共 53 条
[1]  
A.C.D. Inc, 2019, ACD 1 LAB 2 0 VERS 5
[2]   Relationship between quantitative assessments of salivary buffering capacity and ion activity product for hydroxyapatite in relation to cariogenic potential [J].
Aiuchi, H. ;
Kitasako, Y. ;
Fukuda, Y. ;
Nakashima, S. ;
Burrow, M. F. ;
Tagami, J. .
AUSTRALIAN DENTAL JOURNAL, 2008, 53 (02) :167-171
[3]   Application of biorelevant saliva-based dissolution for optimisation of orally disintegrating formulations of felodipine [J].
Ali, Joseph ;
Zgair, Atheer ;
Hameed, Ghaidaa S. ;
Garnett, Martin C. ;
Roberts, Clive J. ;
Burley, Jonathan C. ;
Gershkovich, Pavel .
INTERNATIONAL JOURNAL OF PHARMACEUTICS, 2019, 555 :228-236
[4]   The latest trends in the taste assessment of pharmaceuticals [J].
Anand, Vikas ;
Kataria, Mahesh ;
Kukkar, Vipin ;
Saharan, Vandana ;
Choudhury, Pratim Kumar .
DRUG DISCOVERY TODAY, 2007, 12 (5-6) :257-265
[5]  
Andreev A, 2016, PROC CONF OPEN INNOV, P3, DOI 10.23919/FRUCT.2016.7892176
[6]  
Aulton's A.M., 2007, PHARMACEUTICS
[7]  
Banakar U.V., 1991, PHARM DISSOLUTION TE, DOI 10.1201/b14198
[8]   The buffer capacity and buffer systems of human whole saliva measured without loss of CO2 [J].
Bardow, A ;
Moe, D ;
Nyvad, B ;
Nauntofte, B .
ARCHIVES OF ORAL BIOLOGY, 2000, 45 (01) :1-12
[9]   Formulations for children: problems and solutions [J].
Batchelor, Hannah K. ;
Marriott, John F. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2015, 79 (03) :405-418
[10]  
BENARDE MELVIN A., 1956, JOUR DENTAL RES, V35, P326, DOI 10.1177/00220345560350022801