Sweetening Agent

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Mufrod Mufrod - One of the best experts on this subject based on the ideXlab platform.

  • optimatization of sucrose and aspartame composition as Sweetening Agent in mengkudu fruit ethanolic extract effervescent tablet formulation
    Current Opinion in Organ Transplantation, 2015
    Co-Authors: Galih Pratiwi, Triana Hertiani, Mufrod Mufrod
    Abstract:

    Mengkudu ( Morinda citrifolia L. ) has been widely used as traditional medicine. Its unpleasant smell and flavor urge a more acceptable dosage formulation. The aim of this research was to optimize the composition of sucrose and aspartame as Sweetening Agent in effervescent tablet formulation by using Simplex Lattice Design method. Effervescent tablets were produced by fusion method in five (5) different formulas, i.e. formula I (100% sucrose), II (suucrose-aspartame=75%:25%), III (sucrose-aspartame=50%:50%), IV (sucrose-aspartame=25%:75) dan V (100% aspartame). Effervescent granules were evaluated for mass density, flowing time, tapping index and compactibility characteristics. The effervescent tablets were tested for weight uniformity, hardness, friability, and disintegration time characteristics as well as TLC profile chromatogram. Data was analyzed by one way ANOVA, Scheffe method and Kruskall-Wallis with significance level 95%. The tablet acceptability was tested among 30 respondents. The results showed that the different composition of sucrose-aspartame influence the physical characteristics of granules and tablets effervescent produced. More sucrose content will increase the hardness, lower the friability but prolong the disintegration time. 70% respondents chose formula III as the best formula. Evaluation of SLD data recommended sucrose and aspartame in 42:58 proportion as the most optimum formula.

Fernando Coelho - One of the best experts on this subject based on the ideXlab platform.

Ayoade Lateef Adejumo - One of the best experts on this subject based on the ideXlab platform.

Xia Zhang - One of the best experts on this subject based on the ideXlab platform.

  • Identification wild and cultivated licorice by multidimensional analysis.
    Food chemistry, 2020
    Co-Authors: Wang Hanqing, Weiwei Tao, Wen Song, Juanhong Zhang, Xia Zhang, Zhao Jianjun, Yong Jingjiao, Gao Xiaojuan, Lan-ping Guo
    Abstract:

    Licorice is known as a botanical source in medicine and a Sweetening Agent in food products. Commercial licorice is from the source of wild and cultivated G. uralensis. It was recognized that the material basis of wild and cultivated licorice is different. This study systematically investigated the difference between them by multidimensional analysis technology. The results showed that the content of starch grain, total dietary fibre (TDF), and 11 secondary metabolite components was significantly different in wild and cultivated licorice. principal component analysis (PCA) and orthogonal partial least square (OPLS-DA) analyses showed that the wild and cultivated licorice samples could be clearly separated based on the acquired data of microscopic, macromolecular substance and secondary metabolite analysis. The main markers were starch grain, isoliquiritin apioside, liquirtin apioside and TDF. Additionally, NIR spectroscpy combined with PLS-DA has demonstrated a suitable, fast and nondestructive methodology for authentication of wild and cultivated licorice.

  • identification of metabolites of liquiritin in rats by uhplc q tof ms ms metabolic profiling and pathway comparison in vitro and in vivo
    RSC Advances, 2018
    Co-Authors: Xia Zhang, Caijuan Liang, Jintuo Yin, Yupeng Sun, Lantong Zhang
    Abstract:

    Liquiritin (LQ), the main bioactive constituent of licorice, is a common flavoring and Sweetening Agent in food products and has a wide range of pharmacological properties, including antidepressant-like, neuroprotective, anti-cancer and anti-inflammatory properties. This study investigated the metabolic pathways of LQ in vitro (rat liver microsomes) and in vivo (rat model) using ultra high-performance liquid chromatography coupled with hybrid triple quadrupole time-of-flight mass spectrometry (UHPLC-Q-TOF-MS/MS). Moreover, supplementary tools such as key product ions (KPIs) were employed to search for and identify compounds. As a result, 56 in vivo metabolites and 15 in vitro metabolites were structurally characterized. Oxidation, reduction, hydrolysis, methylation, acetylation, and sulfate and glucuronide conjugation were determined to be the major metabolic pathways of LQ, and there were differences in LQ metabolism in vitro and in vivo. In addition, the in vitro and in vivo metabolic pathways were compared in this study.

Galih Pratiwi - One of the best experts on this subject based on the ideXlab platform.

  • optimatization of sucrose and aspartame composition as Sweetening Agent in mengkudu fruit ethanolic extract effervescent tablet formulation
    Current Opinion in Organ Transplantation, 2015
    Co-Authors: Galih Pratiwi, Triana Hertiani, Mufrod Mufrod
    Abstract:

    Mengkudu ( Morinda citrifolia L. ) has been widely used as traditional medicine. Its unpleasant smell and flavor urge a more acceptable dosage formulation. The aim of this research was to optimize the composition of sucrose and aspartame as Sweetening Agent in effervescent tablet formulation by using Simplex Lattice Design method. Effervescent tablets were produced by fusion method in five (5) different formulas, i.e. formula I (100% sucrose), II (suucrose-aspartame=75%:25%), III (sucrose-aspartame=50%:50%), IV (sucrose-aspartame=25%:75) dan V (100% aspartame). Effervescent granules were evaluated for mass density, flowing time, tapping index and compactibility characteristics. The effervescent tablets were tested for weight uniformity, hardness, friability, and disintegration time characteristics as well as TLC profile chromatogram. Data was analyzed by one way ANOVA, Scheffe method and Kruskall-Wallis with significance level 95%. The tablet acceptability was tested among 30 respondents. The results showed that the different composition of sucrose-aspartame influence the physical characteristics of granules and tablets effervescent produced. More sucrose content will increase the hardness, lower the friability but prolong the disintegration time. 70% respondents chose formula III as the best formula. Evaluation of SLD data recommended sucrose and aspartame in 42:58 proportion as the most optimum formula.