PJPatcharawalai Jaisamut

Patcharawalai Jaisamut

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

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Patcharawalai Jaisamut has a total of 42 co-authors. Here are the top co-authors by number of shared publications:


Latest Publications

  • Open Access

    Leveraging Transfer Learning for Tri-Dhat Classification of Tongue Images in Traditional Thai Medicine

    by Kasikrit Damkliang, Teerawat Sudkhaw, Thitinan Yingtawee, Nasma Saearma, Kotchakorn Moosigapong, Patcharawalai Jaisamut, Julalak Chokpaisarn, Sirinat Laman, Anintita Intan, Anyamanee Ladam

    Traditional Thai medicine (TTM) is a popular and increasingly accepted treatment option. In TTM, tongue diagnosis is a highly efficient method for assessing overall health, yet its accuracy can vary significantly depending on the practitioner's expertise. In this work, we hypothesize that deep learning-based transfer learning (TL) methods can achieve high accuracy in the Tri-Dhat classification of tongue images, a system that aligns with TTM principles and categorizes the tongue into three types: Vata, Pitta, and Kapha. We propose an approach that uses raw pixel data and artificial intelligence (AI) to support TTM diagnoses. For our analysis, we used a unique dataset of genuine tongue images collected from our university's TTM hospital. To prepare the data, we performed class balancing and data augmentation. We then developed TL techniques with a variety of pretrained deep learning models. For performance comparisons, we utilized two-tailed paired t-tests and single-factor ANOVA. Our experiments showed that the DenseNet121 and Xception models produced the most significant results with cropped image datasets, including both DSLR- and mobile-taken images. Notably, an ensemble of these models yielded the highest average predictions. This ensemble achieved an accuracy of 0.96, a precision of 0.94, an F1 score of 0.96, a sensitivity of 0.96, and a specificity of 0.97. These results were further supported by a p-value of 0.0003 from the ANOVA analysis. We suggest that our methods could be effectively deployed in real-world scenarios to aid TTM practitioners in their diagnoses.


  • Open Access

    Safety Evaluation of the Polyherbal Formulation NawaTab: Acute and Subacute Oral Toxicity Studies in Rats

    by Apichaya Niyomchan, Wasapon Chatgat, Bodin Chatawatee, Thaweeporn Keereekoch, Acharaporn Issuriya, Patcharawalai Jaisamut, Sasitorn Chusri, Nongluk Kunworarath

    NawaTab is a tablet formulation developed from the Nawametho polyherbal formula used in Surat Thani province, Southern Thailand, for the treatment of hyperlipidemia. This study aims at evaluating the acute and subacute toxicity of NawaTab in rats. In the acute toxicity study, NawaTab was evaluated in female rats following the OECD Guideline No. 423. In the subacute toxicity study, NawaTab was tested in both male and female rats following the OECD Guideline No. 407. In the acute toxicity study, no lethal effects or toxic signs were observed during the duration of the study. In the subacute toxicity study, there was no mortality and no abnormality in clinical signs, body weight, food consumption, relative organ weight, and hematological parameters of NawaTab‐treated rats. Significantly increased water consumption by male rats (500 mg/kg BW) and female rats (250, 500, and 1000 mg/kg BW) was observed. In addition, globulin and total cholesterol of female rats (1000 mg/kg BW) significantly increased. These alterations were within normal physiological ranges. Moreover, necropsy and histopathological findings of NawaTab‐treated rats demonstrated no obvious alterations attributable to NawaTab administration. The present study revealed that NawaTab has no significant acute oral toxicological effects. The lethal dose with a 50% mortality rate (LD50) was higher than 5000 mg/kg BW in rats. The subacute oral administration of NawaTab for 28 days did not have any major toxicological effects. Based on this study, NawaTab could be safe to use with caution pending its chronic toxicity study.


  • Open Access

    Supplementation with the Traditional Thai Polyherbal Medicine NawaTab Ameliorates Lipid Profiles in High-Fat Diet-Induced Hyperlipidemic Rats

    by Apichaya Niyomchan, Wasapon Chatgat, Bodin Chatawatee, Thaweeporn Keereekoch, Patcharawalai Jaisamut, Sasitorn Chusri, Nongluk Kunworarath

    A tablet formulation developed from Nawametho decoction (NawaTab), a traditional Thai herbal mixture described in the Worayokasan scripture, has been used clinically for several years in the management of borderline hyperlipidemic individuals. Nevertheless, scientific evidence supporting its claims has never been identified. This study aimed to describe the antihyperlipidemic properties of NawaTab in a well-described model of high-fat diet (HFD)-induced hyperlipidemic rats. Decoction of Nawametho containing equal quantities of Aegle marmelos (L.), Carthamus tinctorius L., Hibiscus sabdariffa Linn., Phyllanthus emblica L., Piper longum L., Piper nigrum L., Terminalia bellirica (Gaertn.) Roxb., Terminalia chebula Retz., and Zingiber officinale Roscoe were prepared. The HFD-fed rats were administered NawaTab for 4 consecutive weeks starting from the ninth week of HFD treatment at a dose of 125mg/kg (p.o.). Anthropometric parameters, serum lipid profiles, lipase activity, and liver and renal functional markers were measured. Histopathological examination of the liver and any steatosis was carried out at the end of this study. Consecutive treatment with NawaTab (125mg/kg/day) in HFD-induced hyperlipidemic rats caused a significant reduction in serum total cholesterol, triglyceride, low-density lipoprotein cholesterol, and very low-density lipoprotein cholesterol levels. However, at the tested dose, NawaTab failed to prevent the onset of hepatic steatosis and adipose tissue accumulation. No adverse events due to the consumption of NawaTab on liver and kidney function markers were noted. These findings are the first suggestive evidence for the lipid-lowering capability of NawaTab. However, to promote the use of this formulation in the management of borderline hyperlipidemic patients, elucidation of the underlying mechanisms of action, quantification of biological markers, and clinical trials of NawaTab are urgently needed.


  • Open Access

    Clinical Evaluation of a Novel Tablet Formulation of Traditional Thai Polyherbal Medicine Named Nawametho in Comparison with Its Decoction in the Treatment of Hyperlipidemia

    by Patcharawalai Jaisamut, Channong Tohlang, Subhaphorn Wanna, Acharaporn Thanakun, Thawatchai Srisuwan, Surasak Limsuwan, Wissava Rattanachai, Jarinee Suwannachot, Sasitorn Chusri

    In the traditional medical system in Thailand, medicinal plants and polyherbal medicines have been prescribed as lipid-lowering agents, including Nawametho decoction. This polyherbal formulation is described in the Worayokasan scripture. It consists of nine medicinal plants (Aegle marmelos (L.), Carthamus tinctorius L., Hibiscus sabdariffa Linn., Phyllanthus emblica L., Piper longum L., Piper nigrum L., Terminalia bellirica (Gaertn.) Roxb., Terminalia chebula Retz., and Zingiber officinale Roscoe). Apart from its utilization in Thai traditional medicine, there is a lack of evidence supporting its use. This research work thereby aims to formulate and evaluate the tablet containing Nawametho decoction. The feasibility of Nawametho decoction and NawaTab for patients with borderline hyperlipidemia was additionally examined using a prospective, open-label, randomized, parallel-group design. The dry granulation technique was employed to formulate the polyherbal tablets. The tablets were developed using the spray-dried Nawametho decoction as the active ingredient in addition to other excipients. The chosen formulation, the FB (NawaTab), consisted of 385 milligrams of the extract, 12 w/w of a diluent (lactose), 8 w/w of a lubricant (magnesium stearate), 5 w/w of a disintegrant (microcrystalline cellulose), and 5 w/w of an anti-adherent (talcum). Their hardness, friability, and disintegration time were 4.40.32kg, 0.050.02, and 4.600.05min, respectively. Accelerated stability study results revealed that NawaTab was stable for six months at 40C/75 RH and 25C/60 RH. Even though taking NawaTabs (500mg twice daily) for eight consecutive weeks was unable to improve the lipid profile of the patients, the administration of Nawametho decoction (30mL twice daily) was associated with a significant decrease in serum triglycerides of the patients. The results show that the dry granulation technique is suitable for the formulation of NawaTab based on the tablet evaluation. Furthermore, the triglyceride-lowering effect of Nawametho decoction was reported for the first time.


  • Open Access

    Evaluation of Microwave-Assisted Extraction Method for Preparation and Assessment of Thai Herbal Medicine Oral Tablets With Enriched Phytochemical Compounds

    by Patcharawalai Jaisamut, Subhaphorn Wanna, Atcharaporn Thanakoon, Supanit Saejew, Nutkawan Saowapark, Waramporn Suchato, Preyanuch Chumvong, Tanpisit Kosawiwat, Phonsinee Momaklua, Sasitorn Chusri

    In developing countries, populations have employed herbal medicines for primary health care because they are believed to be more appropriate to the human b


  • Enhanced Oral Bioavailability and Improved Biological Activities of a Quercetin/Resveratrol Combination Using a Liquid Self-Microemulsifying Drug Delivery System

    by Patcharawalai Jaisamut, Subhaphorn Wanna, Surasak Limsuwan, Sasitorn Chusri, Kamonthip Wiwattanawongsa, Ruedeekorn Wiwattanapatapee

    Both quercetin and resveratrol are promising plant-derived compounds with various well-described biological activities; however, they are categorized as having low aqueous solubility and labile natural compounds. The purpose of the present study was to propose a drug delivery system to enhance the oral bioavailability of combined quercetin and resveratrol. The suitable self-microemulsifying formulation containing quercetin together with resveratrol comprised 100 mg Capryol 90, 700 mg Cremophor EL, 200 mg Labrasol, 20 mg quercetin, and 20 mg resveratrol, which gave a particle size of 16.91 ± 0.08 nm and was stable under both intermediate and accelerated storage conditions for 12 months. The percentages of release for quercetin and resveratrol in the self-microemulsifying formulation were 75.88 ± 1.44 and 86.32 ± 2.32%, respectively, at 30 min. In rats, an in vivo pharmacokinetics study revealed that the area under the curve of the self-microemulsifying formulation containing quercetin and resveratrol increased approximately ninefold for quercetin and threefold for resveratrol compared with the unformulated compounds. Moreover, the self-microemulsifying formulation containing quercetin and resveratrol slightly enhanced the in vitro antioxidant and cytotoxic effects on AGS, Caco-2, and HT-29 cells. These findings demonstrate that the self-microemulsifying formulation containing quercetin and resveratrol could successfully enhance the oral bioavailability of the combination of quercetin and resveratrol without interfering with their biological activities. These results provide valuable information for more in-depth research into the utilization of combined quercetin and resveratrol.


  • Open Access

    Antioxidant capacities and total phenolic contents of 20 polyherbal remedies used as tonics by folk healers in Phatthalung and Songkhla provinces, Thailand

    by Wipawee Chanthasri, Nuntitporn Puangkeaw, Nongluk Kunworarath, Patcharawalai Jaisamut, Surasak Limsuwan, Katesarin Maneenoon, Piyapong Choochana, Sasitorn Chusri

    Uses of polyherbal formulations have played a major role in traditional medicine. The present study is focused on the formulations used in traditional Thai folkloric medicine as tonics or bracers. Twenty documented polyherbal mixtures, used as nourishing tonics by the folk healers in Phatthalung and Songkhla provinces in southern Thailand, are targeted. Despite traditional health claims, there is no scientific evidence to support the utilization of polyherbal formulations. The phenolic and flavonoid contents of the polyherbal formulations and a series of antioxidant tests were applied to measure their capability as preventive or chain-breaking antioxidants. In addition, the cytotoxic activity of effective formulations was assayed in Vero cells. Ninety-eight plant species belonging to 45 families were used to prepare the tested formulation. The preliminary results revealed that water extracts of THP-R016 and THP-R019 contain a high level of total phenolic and flavonoid contents and exhibit remarkable antioxidant activities, as tested by DPPH, ABTS, and FRAP assays. The extract of THP-R019 also showed the strongest metal chelating activities, whereas THP-R016 extract possessed notable superoxide anion and peroxyl radical scavenging abilities. The data provide evidence that the water extracts of folkloric polyherbal formulations, particularly THP-R016, are a potential source of natural antioxidants, which will be valuable in the pharmaceutical and nutraceutical industries. The free radical scavenging of THP-R016 may be due to the contribution of phenolic and flavonoid contents. Useful characteristics for the consumer, such as the phytochemical profiles of active ingredients, cellular based antioxidant properties and beneficial effects in vivo, are under further investigation.