Characterization of Hydroxypropyl Tapioca Starch and its Pregelatinized Starch as Tablet Disintegrants
13
Issued Date
2022-05-01
Resource Type
ISSN
00389056
eISSN
1521379X
Scopus ID
2-s2.0-85124564980
Journal Title
Starch/Staerke
Volume
74
Issue
5-6
Rights Holder(s)
SCOPUS
Bibliographic Citation
Starch/Staerke Vol.74 No.5-6 (2022)
Suggested Citation
Charoenthai N., Sanga-ngam T., Kasemwong K., Sungthongjeen S., Puttipipatkhachorn S. Characterization of Hydroxypropyl Tapioca Starch and its Pregelatinized Starch as Tablet Disintegrants. Starch/Staerke Vol.74 No.5-6 (2022). doi:10.1002/star.202100263 Retrieved from: https://repository.li.mahidol.ac.th/handle/123456789/83256
Title
Characterization of Hydroxypropyl Tapioca Starch and its Pregelatinized Starch as Tablet Disintegrants
Author's Affiliation
Other Contributor(s)
Abstract
Hydroxypropyl tapioca starches (HPTS) and pregelatinized hydroxypropyl tapioca starches (PG-HPTS) with different molar substitutions are characterized as tablet disintegrants in comparison with native tapioca starch (NTS). Powder XRD and polarized light microscopy indicates that HPTS is A-type crystalline starch similar to NTS, whereas PG-HPTS is amorphous. Compared to HPTS, an increase in swelling capacity with higher degree of hydroxypropyl substitution is observed with PG-HPTS. All tablets containing NTS, HPTS, and their pregelatinized starches at 5% and 10% show fast disintegration within 8 min. Interestingly, the tablets with disintegration times of less than 30 s are obtained when NTS and HPTS are used. The tablets containing PG-HPTS with higher degree of hydroxypropyl substitution show longer disintegration time and more retarded drug dissolution when compared to those with non-pregelatinized starches. This might be attributed to higher water sorption and subsequent swollen gel formation of PG-HPTS. The effect of hydroxypropylation on tablet disintegration and dissolution is clearly observed with PG-HPTS. The results revealed that the functionality of PG-HPTS is dependent on the degree of hydroxypropyl substitution, but less dependence is observed with HPTS. In conclusion, HPTS and PG-HPTS with different molar substitutions could be used as disintegrants in tablet formulation.