| 000 | 02926nam a22003257a 4500 | ||
|---|---|---|---|
| 003 | OSt | ||
| 005 | 20250710133829.0 | ||
| 008 | 250709b |||||||| |||| 00| 0 eng d | ||
| 040 |
_aTUPM _bEnglish _cTUPM _dTUPM _erda |
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| 050 |
_aBTH TP 370 _bL37 2025 |
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| 100 |
_aLaqui, Emma Angela D. _eauthor |
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| 245 |
_aDevelopment of an effervescent tablet drink utilizing white cabbage (brassica oleracea var. capitata) and native guava (psidium guajava linn)/ _cEmma Angela D. Laqui, Rochelle Mae M. Mendoza, Beram James A. Pasia, Geraldine Mae D. Rivera, and Rj B. Tabasa.-- |
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| 260 |
_aManila: _bTechnological University of the Philippines, _c2025. |
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| 300 |
_aix, 231pages: _c29cm. |
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| 336 | _2rdacontent | ||
| 337 | _2rdamedia | ||
| 338 | _2rdacarrier | ||
| 500 | _aBachelor's thesis | ||
| 502 |
_aCollege of Industrial Technology.-- _bBachelor of science in food technology; _cTechnological University of the Philippines, _d2025. |
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| 504 | _aIncludes bibliographic references and index. | ||
| 520 | _aThe oversupply of white cabbage and underutilization of native guava in the Philippines presents an opportunity for innovation. These raw materials were utilized to develop innovative, easy-to-drink effervescent tablets. The research involves processing, formulating, analyses, packaging, and sensory evaluation of white cabbage and native guava effervescent tablets. Both ingredients underwent freeze-drying and were combined with excipients to develop a tablet drink. Each tablet averages 1.77 grams in weight, with dimensions of 3.3 mm thickness and 25.3 mm diameter. Microbial testing showed acceptable levels based on FDA standards; 1x10 CFU/g APC, <1.1 MPN/ml Coliforms, and 1x10 CFU/g for yeast and molds. The shelf-life analysis utilized microbial accelerated testing, which is equivalent to one month shelf life, with no significant changes in microbial count during the two-week observation period. The product exhibits a substantial vitamin C content of 30.96% (1.0836g). However, the moisture content was 8.64% for the first retest and 7.10% for the second retest. Additionally, the effervescent tablet was within a standard disintegration time in hot water, room temperature, and with a shaker, but exceeded the recommended limits in cold water due to several factors like the particle size, excipients use, the tablet density, and the main raw materials used. Sensory evaluation by untrained panelists has an overall mean of 7.48, interpreted as “Like Very Much”. Trained panelists also deemed the product acceptable and provided valuable insights for improvement. | ||
| 650 | _aEffervescent tablet | ||
| 650 | _aMoisture content | ||
| 650 | _aMicrobial testing | ||
| 700 |
_aMendoza, Rochelle Mae M. _eauthor |
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| 700 |
_aPasia, Beram James A. _eauthor |
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| 700 |
_aRivera, Geraldine Mae D. _eauthor |
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| 700 |
_aTabasa, Rj B. _eauthor |
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| 942 |
_2lcc _cBTH CIT _n0 |
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| 999 |
_c30244 _d30244 |
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