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Featured researches published by Sunibhond Pummangura.


Phytochemical Analysis | 2009

A simple isocratic HPLC method for the simultaneous determination of curcuminoids in commercial turmeric extracts

Wisut Wichitnithad; Nutthapon Jongaroonngamsang; Sunibhond Pummangura; Pornchai Rojsitthisak

INTRODUCTION Turmeric (Curcuma longa) extracts contain three curcuminoids (curcumin, desmethoxycurcumin and bisdesmethoxycurcumin) as major bioactive substances. Previously reported HPLC-UV methods for the determination of curcuminoids have several disadvantages, including unsatisfactory separation times, poor resolution and/or complicated solvent mixtures with gradient elution. OBJECTIVE To develop a simple isocratic HPLC-UV method for the simultaneous determination of individual curcuminoids for the quality control of turmeric extracts. METHODOLOGY The sample was prepared by dissolving the extract in acetonitrile and subsequently diluting with 50% acetonitrile. This solution was analysed by reverse-phase chromatography on an Alltima C(18) column with isocratic elution of acetonitrile and 2% v/v acetic acid (40:60, v/v) at a flow rate of 2.0 mL/min, a column temperature of 33 degrees C, and UV detection at 425 nm. The method was validated and applied for quantification of individual curcuminoids in commercial turmeric extracts. RESULTS The method allowed simultaneous determination of curcumin, desmethoxycurcumin and bisdesmethoxycurcumin in the concentration ranges of 10-60, 4-24 and 0.5-3.0 microg/mL, respectively. The limits of detection and quantification were, respectively, 0.90 and 2.73 microg/mL for curcumin, 0.84 and 2.53 microg/mL for desmethoxycurcumin and 0.08 and 0.23 microg/mL for bisdesmethoxycurcumin, and the percentage recoveries were, respectively, 99.16-101.75 (%RSD < or = 1.11%), 99.50-101.01 (%RSD < or = 1.74%) and 99.67-101.92 (RSD < or = 1.31%). CONCLUSION The method was found to be simple, accurate and precise and is recommended for routine quality control analysis of turmeric extracts containing the three curcuminoid compounds as the main principles in the herb.


Drug Development and Industrial Pharmacy | 1994

Chitin and Chitosan as Disintegrants in Paracetamol Tablets

Garnpimol C. Ritthidej; Parichat Chomto; Sunibhond Pummangura; Piamsak Menasveta

AbstractChitin and chitosan as disintegrants in paracetamol tablets were evaluated and compared to four commonly used disintegrants. Tablets containing chitosan showed faster disintegration, greater dissolution and was slightly softer than those containing chitin. An increment in concentration of these polymers caused markedly faster disintegration and better dissolution while an increase in compressional force showed opposite effects. Aging slightly altered the disintegration and dissolution. Tablets containing 7% of chitosan disintegrated within one minute which was much faster than those containing corn starch and microcrystalline cellulose but slightly slower than those containing sodium starch glycolate and croscamellose sodium. However, their dissolution profiles were non-significantly different from those of the latter ones.Crystallinity, degree of acetylation, chain length and particle size were attributed to the efficiency of chitin and chitosan. Moisture sorption and water uptake were found to b...


Journal of Natural Products | 2002

Ecteinascidins 770 and 786 from the Thai tunicate Ecteinascidia thurstoni.

Khanit Suwanborirux; Kornvika Charupant; Surattana Amnuoypol; Sunibhond Pummangura; and Akinori Kubo; Naoki Saito


Phytochemistry | 2003

Synthesis and anti-herpes simplex viral activity of monoglycosyl diglycerides

Wicharn Janwitayanuchit; Khanit Suwanborirux; Chamnan Patarapanich; Sunibhond Pummangura; Vimolmas Lipipun; Tirayut Vilaivan


Journal of Natural Products | 2003

Chemistry of Renieramycins. Part 3. 1 Isolation and Structure of Stabilized Renieramycin Type Derivatives Possessing Antitumor Activity from Thai Sponge Xestospongia Species, Pretreated with Potassium Cyanide

Khanit Suwanborirux; Surattana Amnuoypol; Anuchit Plubrukarn; Sunibhond Pummangura; Akinori Kubo; Chieko Tanaka; Naoki Saito


Tetrahedron | 2004

Chemistry of renieramycins. Part 6: Transformation of renieramycin M into jorumycin and renieramycin J including oxidative degradation products, mimosamycin, renierone, and renierol acetate

Naoki Saito; Chieko Tanaka; Yu-ichi Koizumi; Khanit Suwanborirux; Surattana Amnuoypol; Sunibhond Pummangura; Akinori Kubo


Journal of Natural Products | 2004

Chemistry of Renieramycins. Part 5.1 Structure Elucidation of Renieramycin-Type Derivatives O, Q, R, and S from Thai Marine Sponge Xestospongia Species Pretreated with Potassium Cyanide†

Surattana Amnuoypol; Khanit Suwanborirux; Sunibhond Pummangura; Akinori Kubo; Chieko Tanaka; Naoki Saito


Archive | 2007

HPLC determination of active diterpene lactones from Andrographis paniculata Nees planted in various seasons and regions in Thailand

Chamnan Patarapanich; Suwanna Laungcholatan; Nuntakan Mahaverawat; Chaiyo Chaichantipayuth; Sunibhond Pummangura


Heterocycles | 2001

13C NMR Spectral Assignment of 5-Hydroxy-1,5-imino-3-benzazocin-4,7,10-trione Derivatives: The Revised Structure of Renieramycin H

Naoki Saito; Haruyuki Sakai; Khanit Suwanborirux; Sunibhond Pummangura; Akinori Kubo


International Symposium on the Chemistry of Natural Products | 2006

P-572 DEVELOPMENT AND VALIDATION OF A NEW HPLC METHOD FOR THE SIMULTANEOUS DETERMINATION OF CURCUMIN, DEMETHOXYCURCUMIN AND BISDEMETHOXYCURCUMIN IN TURMERIC EXTRACTS

Pornchai Rojsitthisak; Sunibhond Pummangura; Suthatip Chantaraskul; Suwanna Laungchonlatan; Chamnan Patarapanich; Darawan Tanyavutti; Mitr Pathipvanich; Wisut Wichitnithad

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Chieko Tanaka

Meiji Pharmaceutical University

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Ryu-ichi Seki

Meiji Pharmaceutical University

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Yu-ichi Koizumi

Meiji Pharmaceutical University

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