Pimolwan Siriparu

Ms. Pimolwan Siriparu

Faculty of Pharmaceutical Sciences, Khon Kaen University, Khon Kaen, Thailand
orcid

Research Focus & Metrics

Academic Career Length

5Years (2022-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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6 November 2022 in Plants
Verified
Journal Article
Open access
PDF file
PSPimolwan Siriparu
Pimolwan Siriparu
PPPanyada Panyatip
Panyada Panyatip
TPThanawat Pota
Thanawat Pota
JRJuthamat Ratha
Juthamat Ratha
CYChawalit Yongram
Chawalit Yongram
PPPloenthip Puthongking
Ploenthip Puthongking
Mung bean (Vigna radiata L.) sprouts are increasingly consumed and have become part of a healthy diet. The sprouts are composed of proteins, carbohydrates, and biochemical compounds. During germination, the phytochemical compounds are significantly elevated, especially under stress conditions such as salinity, drought, extreme temperature, and illumination. The present study examined the effects of light and germination time on the bioactive compounds in mung bean sprout extracts. Mung bean seeds were sprouted under different light exposure conditions, and the phytochemical composition and antioxidant activity of sprout extracts were determined compared to seeds. The results show that tryptophan sharply decreased during germination. On the contrary, melatonin, polyphenols, and total phenolic content (TPC) were elevated with increased germination time, correlated with increased antioxidant activity. Sprouts germinated in the dark presented higher levels of melatonin and TPC compared with those germinated under 12 h light exposure (3.6- and 1.5-fold, respectively). In conclusion, germination can enhance valuable phytochemicals and antioxidant activity of mung bean sprouts. Mung bean sprouts may be a good alternative functional food for promoting human health.

30 January 2023 in Plants
Verified
Journal Article
Open access
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JRJuthamat Ratha
Juthamat Ratha
CYChawalit Yongram
Chawalit Yongram
PPPanyada Panyatip
Panyada Panyatip
PPPatcharapol Powijitkul
Patcharapol Powijitkul
PSPimolwan Siriparu
Pimolwan Siriparu
PPPloenthip Puthongking
Ploenthip Puthongking
Plants are a rich source of phytochemical compounds with antioxidant activity. Several studies have revealed that the consumption of plant polyphenols reduces the risk of diseases. Purple corn (Zea mays L. variety KND) and butterfly pea (Clitoria ternatea; CT) were selected to be investigated as alternative natural polyphenol sources to increase the value of these plants. Phytochemical profiles and antioxidant activities of KND cob, silk, husk and CT extracts alone and in combination were investigated in this study. The results revealed that purple corn cob (C) extract had the highest tryptophan, melatonin, total anthocyanin (TAC) and delphinidin content, while the purple corn silk (S) extract showed the highest total phenolic content (TPC) and antioxidant activities. Serotonin was found only in purple corn husk (H) extract and C extract. High contents of tryptophan and sinapic acid were found in CT extract. Principal component analysis (PCA) revealed that strong antioxidant activities were strongly correlated with protocatechuic acid and p-hydroxybenzoic acid contents, moderate antioxidant activities were strongly correlated with melatonin, and low antioxidant activities were strongly correlated with sinapic acid content. Therefore, the purple corn variety KND waste cobs, silk and husks are a potentially rich source of health-promoting phytochemical compounds.

7 January 2026 in Plants
Verified
Journal Article
Open access
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JRJuthamat Ratha
Juthamat Ratha
TPTanit Padumanonda
Tanit Padumanonda
CYChawalit Yongram
Chawalit Yongram
PSPimolwan Siriparu
Pimolwan Siriparu
SDSuthida Datham
Suthida Datham
PPPloenthip Puthongking
Ploenthip Puthongking
Sunflower seeds have been reported to be a healthy natural source of polyphenols. This study aimed to explore the mechanisms of potential compounds in sunflower seed extract involved in wound healing; major compounds were investigated through network pharmacology and molecular docking. In an in vitro wound-healing assay applied using an immortalised human keratinocyte (HaCaT) cell model, 10 µg/mL of the sunflower seed extract promoted cell migration in HaCaT cells and led to complete wound closure after 24 h; at a 1 µg/mL concentration, it led to complete wound closure after 72 h. The sunflower seed extract presented moderate-to-strong antioxidant activity. Liquid chromatography–mass spectrometry and high-performance liquid chromatography were used to identify the major compounds present in the sunflower seed extract. Forty-seven compounds were identified, among which chlorogenic acid was the most abundant phenolic compound. Network pharmacology was used to identify wound-healing-related targets. In total, 252 proteins were linked to the 47 compounds. Cyto-Hubba analysis identified 10 hub proteins with a strong correlation with wound healing. Molecular docking was used to assess the ability of the major compounds in the sunflower seed extract to combat NF-κB1, EGFR, and MMP9. Chlorogenic acid showed higher binding affinity to all targets. Moreover, its pharmacokinetic properties were well distributed in the plasma (VDss = 0.377 log L/kg), and they were not a carcinogen and did not cause skin sensitisation. In conclusion, the findings suggest that the sunflower seed extract is a potential source of bioactive compounds that can enhance wound healing and can be developed to create a transdermal application.

2 June 2026 in Plants
Verified
Journal Article
Open access
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PPPloenthip Puthongking
Ploenthip Puthongking
JRJuthamat Ratha
Juthamat Ratha
PSPimolwan Siriparu
Pimolwan Siriparu
MSMuhammad Subhan
Muhammad Subhan
PPPanyada Panyatip
Panyada Panyatip
Bunleu SungthongBunleu Sungthong
Bunleu Sungthong
Plant polyphenols possess various biological activities such as antioxidant and antidiabetic activities. Based on the high plant biodiversity in Thailand, selected edible plants were therefore investigated to explore how dietary polyphenols and α-glucosidase-inhibitory activity can contribute to significant control and prevention of type 2 diabetes mellitus (T2DM). Network pharmacology of antidiabetic activity was employed to predict the underlying antidiabetic mechanisms of the phytochemicals identified in the 15 selected edible Thai plants. The results showed that wild guava (Careya arborea Roxb.; CaA) leaf extract presented the highest total phenolic content (TPC). CaA exhibited the highest antioxidant activities in all the assays as a function of its TPC. Moreover, CaA showed the highest inhibitory effect on α-glucosidase activity in the test, with an IC50 of 0.13 µg/mL, being approximately 1600 times more potent than the standard α-glucosidase-inhibitory drug acarbose. Phenolic profile analysis revealed that the CaA leaf extract consisted of gallic acid, caffeic acid, sinapic acid, rutin, and quercetin. The phytochemical contents of CaA strongly contributed to its antioxidant and α-glucosidase-inhibitory activity. In addition to other phytochemicals, the highest contents of the indolamine compounds tryptophan and melatonin were found in malabar spinach (Basella alba L.; BA) and water clover (Marsilea crenata C. Presl; MaC), at 2213.05 and 99.17 ng/g DW, respectively. Network pharmacology on antidiabetic activity exhibited the most relevant pathway involved in the insulin resistance and AGE-RAGE signaling pathways that caused glucose and glycogen synthesis in skeletal muscle, increasing hepatic gluconeogenesis, and reduced glycogen synthesis in the liver. The implication of these findings is that these Thai edible plants have the potential to combat diabetes by inhibiting the function of α-glucosidase.

Verified
Journal Article
Open access
PDF file
MSMuhammad Subhan
Muhammad Subhan
KSKamonpan Sanachai
Kamonpan Sanachai
BNBodee Nutho
Bodee Nutho
JRJuthamat Ratha
Juthamat Ratha
PSPimolwan Siriparu
Pimolwan Siriparu
PPPloenthip Puthongking
Ploenthip Puthongking
Persicaria odorata (Lour.) contains considerable amounts of phytochemicals, including phenolics and essential oils, which have been reported to inhibit α-glucosidase activity. However, which bioactive compounds play a key role in inhibiting the α-glucosidase activity is unclear. To address this issue, the methanolic extract of P. odorata was assayed via in vitro studies, and forty-four compounds in P. odorata extracts were elucidated using in silico studies. The extract strongly inhibited yeast α-glucosidase with an IC50 value of 0.31 µg/mL, which was 450-fold more potent than acarbose (IC50 = 139.47 µg/mL), under experimental conditions. The Lineweaver–Burk plots indicated that the inhibition type of the extract on α-glucosidase is a noncompetitive inhibitor. Molecular docking demonstrated that procyanidin B (P9) and rutin (P19), which belong to the flavonoids, were predicted by computational approaches to be bioactive compounds that have more favorable binding interactions to yeast α-glucosidase residues compared to forty-four other compounds and acarbose. Molecular dynamics simulations revealed that P9 and P19 complexes with yeast α-glucosidase remained stable during the 500 ns simulations. Moreover, both P9 and P19 were predicted to qualify as α-glucosidase inhibitors with low toxicity. These findings suggest that P. odorata could be used as an alternative edible plant to manage postprandial hyperglycemia in T2DM, and could serve as basic scientific data. Further experimental studies of the pure bioactive compounds are necessary to support these findings.

1 March 2026 in Journal of Pharmacy & Pharmacognosy Research
Verified
Journal Article
Open access
PSPimolwan Siriparu
Pimolwan Siriparu
JRJuthamat Ratha
Juthamat Ratha
PPPloenthip Puthongking
Ploenthip Puthongking
Context: Solid waste from spent coffee grounds (SCG) has sharply increased due to a growing global coffee market. Concerning environmental impact, the value-added of solid waste from coffee drinking, especially in the pharmaceutical industry, was investigated in this research. Aims: To compare the phytochemical content, antioxidant activity, and wound healing properties of Arabica (AB) and Robusta (RB) coffee bean extracts and SCG extracts (AG and RG, respectively). Methods: The total phenolic content (TPC), the total flavonoid content (TFC), high-performance liquid chromatography (HPLC), and gas chromatography–mass spectrometry (GC-MS) were used to analyze the extracts. In addition, the antioxidant and wound healing activities of the extracts were evaluated. Results: The coffee beans showed stronger antioxidant activity than the SCG extract. Robusta exhibited higher antioxidant activity than Arabica, consistent with its higher TPC. HPLC analysis identified melatonin and tryptophan in all samples, with greater concentrations in the coffee bean extracts, especially AB. GC-MS analysis indicated Robusta contained more caffeine. Interestingly, the AG extract had the lowest caffeine content (6.87%) but produced the fastest wound closure (84.8% after 48 h, compared with 77.5% for the control), achieving >98% closure after 72 h. Conclusions: Robusta contained higher antioxidant and polyphenol levels than Arabica, while coffee beans generally possessed more beneficial phytochemicals than spent grounds. However, the AG extract showed the greatest potential for promoting wound healing, suggesting its possible use in biomedical or cosmetic applications.