Jukkarin Srivilai

Dr. Jukkarin Srivilai

orcid

Research Focus & Metrics

Academic Career Length

13Years (2014-Present)

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

Representative Publications

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10 October 2017 in Nutrients
Verified
Journal Article
Open access
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Wantida ChaiyanaWantida Chaiyana
Wantida Chaiyana
CPChanun Punyoyai
Chanun Punyoyai
SSSuvimol Somwongin
Suvimol Somwongin
PLPimporn Leelapornpisid
Pimporn Leelapornpisid
KIKornkanok Ingkaninan
Kornkanok Ingkaninan
MMMonika Mueller
Monika Mueller
This study aims to investigate the biological activities related to hair loss of Equisetum debile extracts, including 5α-reductase inhibition, interleukin-6 (IL-6) secretion reduction, and anti-oxidation. E. debile extracts were obtained by maceration in various solvents. Crude extract (CE) was obtained by maceration in 95% ethanol. Chlorophyll-free extract (CF) was the CE which of the chlorophyll has been removed by electrocoagulation. Hexane extract (HE), ethyl acetate extract (EA), and ethanolic extract (ET) were fraction extracts obtained from maceration in hexane, ethyl acetate, and 95% ethanol, respectively. The extracts were investigated for inhibitory activity against 5α-reductase and IL-6 secretion. Total phenolic contents (TPC) were investigated and antioxidant activities were determined by means of 2,2′-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS), 2,2′-diphenyl-1-picrylhydrazyl (DPPH), and ferric reducing antioxidant power (FRAP) assays. The inhibition of lipid peroxidation was determined by the ferric thiocyanate method. The cytotoxicity of the extracts on dermal papilla cells and irritation test by hen's egg test chorioallantoic membrane assay were also investigated. All extracts could inhibit 5α-reductase and decrease IL-6 secretion in lipopolysaccharide-stimulated macrophage. The antioxidant activity of E. debile extracts was directly related to their TPC. ET which contained the highest TPC (68.8 ± 6.7 mg GA/g) showed the highest equivalent concentration (EC1) of 289.1 ± 26.4 mM FeSO4/g, TEAC of 156.6 ± 34.6 mM Trolox/g, and 20.0 ± 6.0% DPPH inhibition. However, EA exhibited the highest inhibition against lipid peroxidation (57.2 ± 0.4%). In addition, EA showed no cytotoxicity on dermal papilla cell line and no irritation on chorioallantoic membrane of hen’s eggs. In conclusion, EA was suggested as the most attractive ingredients for functional food and nutraceuticals because of the high inhibitory activity against 5α-reductase, IL-6 secretion, and lipid peroxidation inhibition.

1 February 2017 in Phytomedicine
Verified
Journal Article
Closed access
JSJukkarin Srivilai
Jukkarin Srivilai
PPPreeyawass Phimnuan
Preeyawass Phimnuan
JJJiraporn Jaisabai
Jiraporn Jaisabai
NLNantakarn Luangtoomma
Nantakarn Luangtoomma
NWNeti Waranuch
Neti Waranuch
KIKornkanok Ingkaninan
Kornkanok Ingkaninan

20 November 2017 in Drug Delivery and Translational Research
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Journal Article
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JSJukkarin Srivilai
Jukkarin Srivilai
NWNeti Waranuch
Neti Waranuch
ATAnothai Tangsumranjit
Anothai Tangsumranjit
NKNantaka Khorana
Nantaka Khorana
KIKornkanok Ingkaninan
Kornkanok Ingkaninan

21 March 2017 in Medicinal Chemistry Research
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Journal Article
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JSJukkarin Srivilai
Jukkarin Srivilai
KRKarma Rabgay
Karma Rabgay
NKNantaka Khorana
Nantaka Khorana
NWNeti Waranuch
Neti Waranuch
NNNitra Nuengchamnong
Nitra Nuengchamnong
KIKornkanok Ingkaninan
Kornkanok Ingkaninan

1 March 2019 in ASSAY and Drug Development Technologies
Verified
Journal Article
Closed access
JSJukkarin Srivilai
Jukkarin Srivilai
GMGenet Minale
Genet Minale
CSC. Norman Scholfield
C. Norman Scholfield
KIKornkanok Ingkaninan
Kornkanok Ingkaninan
Human steroid 5 alpha-reductases (S5αRs) and NADPH irreversibly reduce testosterone to the more potent dihydrotestosterone (DHT). S5αR inhibitors are useful treatments for DHT-dependent diseases, including benign prostatic hyperplasia, androgenic alopecia and hair growth, and acne. There are three S5αR isozymes, and there is a need for safer and more isozyme selective inhibitors than finasteride and dutasteride currently licensed. In this study, we review the methods used to screen for S5αR inhibitory activity and describe studies that characterize the ability of herbal preparations and their constituents to inhibit S5αRs. We identified enormous variations between studies in IC50s for finasteride and dutasteride used as standards. Accordingly, we make several recommendations: Stable isozyme specific transfection systems need creating a standardized enzyme/microsome preparation and all three isozymes, as well as androgen receptor binding, should be tested; agreed reaction conditions, especially the substrate concentrations, and separation/quantitation method optimized for high throughput screening; systematic screening of herbal compounds and most extensive use of leads to develop more potent and isozyme specific inhibitors.

1 March 2023 in Cosmetics
Verified
Journal Article
Open access
PDF file
TRTammanoon Rungsang
Tammanoon Rungsang
JSJukkarin Srivilai
Jukkarin Srivilai
PRPawarit Rakasawapokin
Pawarit Rakasawapokin
PRPatpitcha Rakasawapokin
Patpitcha Rakasawapokin
LMLapatrada Mungmai
Lapatrada Mungmai
EWEakkaluk Wongwad
Eakkaluk Wongwad
Dendrobium sulcatum Lindl or “Ueang Jampa-Nan” (Orchidaceae family) is widely dis-tributed in Thailand and Laos. It is classified in the genus Dendrobium, which is used in both traditional Chinese medicine and Ayurvedic medicine for health enhancement and anti-aging. The purpose of this study was to investigate the phytochemical constituents and bioefficacy of stems, leaves and flowers from D. sulcatum for cosmetic and cosmeceutical applications. Phenolic and flavonoid contents were tested for the phytochemical evaluation. The antioxidant (DPPH, FRAP and ABTS assays), anti-lipid peroxidation, antiglycation, anti-inflammatory and anti-tyrosinase properties were assessed for their bioefficacy. The results showed that the extracts of stem and leaf had higher total phenolic content than that of the flower, and the leaf extract had the highest flavonoid content. The antioxidant, anti-lipid peroxidation and anti-inflammatory activities of the extracts were greater in those from the stem and leaf compared with that of the flower. The leaf extract exhibited the greatest antiglycation property. The results of anti-tyrosinase analysis of the extracts showed that the leaf and flower exhibited potent activities with a percentage inhibition greater than 70% (at a concentration of 50 µg/mL). In conclusion, these findings suggest that the ethanolic extracts from different parts of D. sulcatum are promising sources of natural active ingredients for further cosmetic and cosmeceutical products.