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GAS Chromatography Mass Spectroscopic Analysis Ayyappala Kera Thailam

Journal of Research in Medical and Dental Science
eISSN No. 2347-2367 pISSN No. 2347-2545

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Research - (2022) Volume 10, Issue 4

GAS Chromatography Mass Spectroscopic Analysis Ayyappala Kera Thailam

*Correspondence: Vijayakumar R, Department of Physiology, Sree Lakshmi Narayana Medical College and Research Institute, Pondicherry, India, Email:

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Abstract

The Gas Chromatography Mass Spectroscopic analysis of one skin care oil Ayyappala Kerathailamand to correlate its medicinal activity with the biomolecules present in it. Some important biomolecules such as Octanoic Acid, n- Octanoic acid, cycobutyl ester, Tetra decanoic acid, Dodecanoic acid, n-Butyl laurate, Dodecanoic acid, pentafluorophenyl ester, Dodecanoic acid, 1-(hydroxymethyl)-1,2-ethanediyl ester, Sarcosine, N-(1-naphthoyl)-, butyl ester, trans-3-Trifluoromethyl cinnamic acid, 4-nitrophenyl ester, 1,3,2-Dioxaphosphorinan-2-amine, 4-methyl-N-phenyl-, 2-oxide, trans-, Dodecanoic acid, ethenyl ester, Acetic acid, cesium salt etc. which have properties supporting the skin treatment role of this oil.

Keywords

Ayyappala kera thailam, GC MS, Ayurvedic, Octadecanoic acid, Octanoic acid, Sarcosine, N-(1-naphthoyl)

Introduction

The validation of traditional and alternative medicines like, Ayuveda, Sidhha, Unani, Chinese etc. by modern scientific parameters is very important to establish their authenticity. This has become all the more pertinent due to the failures of modern day molecular medicines at various fronts. The uses of traditional medicines are in vogue around the globe but due to lack of proper validation they are not coming into the main stream of medicinal practice. Since last decade or so there has been some studies in this regard which is heartening [1-17]. Use of Ayurvedic, Sidhha and other complementary and alternative medicines is an age old practice. The process of preparing of these medicines is also quite elaborate strictly as per the standard procedures and protocols present in the respective literatures.

This report indicates the phytochemicals present in Ayurvedic oil, AyyappalaKerathailam, used for treating psoriasis, chronic exfoliating dermatitis, allergic dermatitis, dermatophytosis, eczema, fungal infections etc. which is used by external application.

The ingredients of this medicine:

KeraTaila: Coconut (Cocos nucifera) oil: 10 ml.

ShwetaKutaja: Wrightia tinctoria leaves: 40 gm.

Nimba: Neem: Azadirachta indica leaves: 1.250 gm.

The oil is applied on the affected skin ½ to one hr. and washed off with warm water. The shelf life is mentioned to be 3 years.

The three ingredients are known for their medicinal values and are in use in various compositions in many Ayurvedic and Sidhha medicines. A brief description of the medicinal potential of each is mentioned hereunder.

Coconut: Cocos nucifera

Coconut is an important cash crop and widely used as a part of food and its beneficial roles are reported by many research articles [18-29]. The use of coconut oil as dietary oil is a common practice in all he countries where coconut is available in plenty. Coconut oil is an important ingredient in most of the Ayurvedic and Sidhha medicines both for intake as well for topical application and one of the most used hair oils. It is considered as one of the best antiseptic for any skin injury.

Wrightia tinctoria

Nimba (Neem): Azadirachta indica

Neem is also a known medicinal plant with wide range of curative roles [30,31]. Thus is it interesting that the Ayurvedic proponents have chosen these three plants to formulate one skin oil for various types of skin ailments only for topical use. The present study is to find the molecular profile of this thailam by Gas Chromatography Mass Spectroscopic analysis. This knowledge could indicate the underlying medicinal properties of this medicine.

Materials and Methods

The medicine Ayyappalakerat hailam was procured from standard Ayurvedic vendor at Chennai, India. 50 ml of Ayyappala kera thailam was taken and extracted with ethyl acetate solvent in separating funnel. The extracted material was filtered and concentrated in water bath at low temperature and was charged to have GC MS patterns by standard procedures.

Mass Spectrometer is used for the determination of molecular weight of the compound and also for their structure elucidation. The compounds are identified by (NIST & WILEY) library.

Results and Discussion

Figure 1 shows the Gas Chromatography Mass S graphs of Ayyapala kera thailam showing the number of peaks, their retention time etc. Table 1 indicates the presence of possible types of compounds with the retention times, molecular mass, peak areas and their medicinal roles found the GC MS profile of Ayyapala kera thailam. The identification of molecules was done NIST spectral library and the possible pharmaceutical roles of each bio-molecule as per National Agriculture Library, USA and others as shown in Table 1. [32]

Sl. No Retention Time Compound Name Mol. Formula Mol. Weight Peak Area Medicinal Role
1 4.32 Octanoic acid C8H1602 144 321692208 Acidifier, Acidulant, Arachidonic acid inhibitor, Inhibits production of uric acid
2 5.02 4-Acetoxy-3-methoxystyrene C11H1203 192.1 37195742 Not Known
3 5.23 n-Decanoic acid C10H2O2 172.1 229614364 Increases production of Uric acid, Anaphylactic, Antitumor, Decreases nor epinephrine production, GABAerigic, Increases NK cell Activity, Myoneuron stimulant
4 6.11 Dodecanoic acid C12H24O2 200.2 948463036 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid
5 6.55 Octanoic acid, cycobutyl Ester C12H22O2 198.2 32880864 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid,
6 6.83 Tetra decanoic acid C14H29O2 228.2 528148778 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid
7 7.94 Dodecanoic acid C12H24O2 200.2 319253420 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid,
8 8.87 Dodecanoic acid, 2,3-dihydropropyl ester C15H30O4 274.2 218939823 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid
9 9.2 1,1’-Bicyclopropyl, 2,2,3,’,2’-tetramethyl- C10H18 138.1 207289051 Not known
10 9.36 3-methylpenta-3-yl propyl carbonate C10H20O3 188.1 70596240 Not Known
11 12.45 Heptane,4-ethyl- C9H20 128.2 55568269 Not Known
12 13.06 1,2-Benzenediol,O-(5-chlorovaleryl)-o’-(1-nephthoyl)- C22H19ClO4 382.1 40675250 Not Known
13 14.79 n-Butyl laurate C16H32O2 256.2 580692387 Anaphylactic, antitumor, Decreases Norepinephrine production, Down regulates nuclear and cytosol androgen production, GABA-ergic, Increases NK cell activity, Inhibits production of Tumor necrosis factor, Myoneuro stimulant, N-Cholinolytic, NADH-Oxidase inhibitor, NADH-Ubiquinone-Oxidoreductase Inhibitor, Narcotic, CNS depressant
14 14.8 Acetic anhydride C4H6O3 102 36264325 Not known
15 16.61 Dodecanoic acid, pentafluorophenyl ester C18H23F5O2 306.2 363369333 Increases production of Uric acid
16 18.39 Dodecanoic acid, 1-(hydroxymethyl)-1,2-ethanediyl ester C27H52O5 456.4 101484340 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid
17 18.42 Sarcosine, N-(1-naphthoyl)-, butyl ester C18H21NO3 299.2 40670803 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid, Anaphylactic, Antitumor, Decrease nor epinephrine production, GABAnerigic, Increases NK cell Activity, Myoneuron stimulant
18 18.47 Caprylic anhydride C16H30O3 270.2 130419195 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid,
19 18.6 Dodecanoic acid, 1-(hydroxymethyl)-1,2-ethanediyl ester C27H52O5 456.4 141767308 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid,
20 19.97 trans-3-Trifluoromethylcinnamic acid, 4-nitrophenyl ester C27H52O5 227.1 32750819 Nitric Oxide Synthase Inhibitor, Catachol-O- Methyl Transferase Inhibitor, Decreases Glutamate Pyruvate Transaminase, Glutathione-S-Transferase Inhibitor
21 20.01 1,3,2-Dioxaphosphorinan-2-amine, 4-methyl-N-phenyl-, 2-oxide, trans- C16H10F3NO4 227.1 81599860 Nitric Oxide Synthase Inhibitor, Catachol O Methyl Transferase Inhibitor, Increases Glutathione S transferase Activity, Catechol O Methyl Transferease Inhibitor, Arachidonic Acid Inhibitor, Decreases Glutamate Pyruvate transaminase, Inhibits Uric acid Production, Acidulant
22 20.09 Dodecanoic acid, ethenyl ester C14H26O2 226.2 824940857 Reverse Transcriptase inhibitor, Increases Glyoxalate transamination, Increases Glutathione S transferase Activity, Catechol O Methyl Transferease Inhibitor, Arachidonic Acid Inhibitor, Decreases Glutamate Pyruvate transaminase, Inhibits Uric acid Production, Acidulant
23 22.41 4-Methyl-2,4-bis(4'-trimethylsilyloxyphenyl)pentene-1 C24H36O2Si2 412.2 2958093897 Catechol-o-methyl Transferease
24 22.94 Acetic acid, cesium salt C2H3CsO2 195.9 107062504 Increases aromatic Amino Acid decarboxylase Activity, Increases production of Uric acid,
medical-dental-Thailam

Figure 1: Indicates the GC MS profile of Ayyappala kera Thailam.

From Figure 1 and Table 1 it is indicated that Ayyapala Kera Thailam contains mostly fatty acids and their esters or salts such as Octanoic Acid, n-Decanoic acid, Dodecanoic acid, Octanoic acid, cycobutyl ester, Tetra decanoic acid, Dodecanoic acid, Dodecanoic acid 2,3-dihydropropyl ester, n-Butyl laurate, Dodecanoic acid, pentafluorophenyl ester, Dodecanoic acid, 1-(hydroxymethyl)-1,2-ethanediyl ester, Sarcosine, N-(1-naphthoyl)-, butyl ester, trans- 3-Trifluoromethyl cinnamic acid, 4-nitrophenyl ester, 1,3,2-Dioxaphosphorinan-2-amine, 4-methyl-N-phenyl-, 2-oxide, trans-, Dodecanoic acid, ethenyl ester, 4-Methyl- 2,4-bis(4'-trimethylsilyloxyphenyl)pentene-1, Acetic acid, cesium salt etc.

The basic concept of Ayurvedic treatment for any disease is to correct the aberration in the three doshas, namely, Vata, Pitha and Kapha. Skin diseases, particularly inflammation and infections are caused due to imbalance in Pitta form of constitution. Coconut oil is considered best in balancing this dosha. It is a coolant andantimicrobial due to the presence of saturated fatty acids, Wrightiatinctoria helps in alleviating all the three doshas. Neem is one of the oldest medicine for skin diseases and also known to have extremely high antibacterial, antiviral and anti-inflammatory activities. The medicinal values of most of the molecules as seen in the GCMS analysis indicate antioxidant, antiinflammatory and antibacterial properties. The possible positive role of some of the molecules are mentioned hereunder:

â?? N Hexadacoinc acid has been reported to have properties such as increase aromatic Amino Acid decarboxylase activity, decrease nor epinephrine production, GABA-nergic, increase NK cell activity and myo-neuron stimulant etc. Increase in aromatic Amino acid decarboxylase activity leads to decarboxylation of L-Dopa and 5-hydroxytryptophan thus increasing the production of catechol amines such as Dopamine, norepinephrine, epinephrine and Serotonin. The presence of more catechol amines cause mood elevation, stress relief and increased peripheral blood circulation. It is neither interesting that this compound decreases the neither function of nor epinephrine, which is known for peripheral vascular contraction. The capacity to stimulate myoneurons also plays a major factor in maintaining good health of skin.

â?? 2-Methyl-3-93-methyl-but-2-enyl)-enyl)-oxetane, has the following biological roles: Catecholo- methyl Transferase inhibitor, Methyl donor, Methyl Guanidine inhibitor etc. Catechol-omethyl Transferase is as enzyme that degrades catechol amines like dopamine, nor epinephrine, epinephrine and other catechol compounds. By inhibiting its activity this compound present in AyyappalaKerathailam makes these compounds available which help in maintaining good health of skin.

â?? 3, 7-Decadien-2-one, 10-(3,3-dimethoxyloxiran dimethyl-, (E,E)-,+/-.- has properties such as anticancer, antidote, antitumor, Cytochrome –P450- 2E1-inhibitor, decreases endothelial leukocyte adhesion, decreases epinephrine production. These properties can indirectly help in maintaining health of skin.

â?? 5α-reductase Inhibitors helps in stoppage of the steroid breakdown thus enabling the availability of the steroid in blood stream which in turn could help maintain the good health of skin.

â?? Alcohol dehydrogenase inhibitor stops the interconversion of alcohols and aldehydes, making them available during glucose metabolism and the presence of this enzyme can increase the energy supply to the skin. Thus it can be surmised from the above discussion it is clear that Ayyappalakerathailam is an excellent medicine for various skin diseases.

Conclusion

Thus it can be surmised from the above discussion it is clear that Ayyappalakerathailam is an excellent medicine for various skin diseases. The biological roles of some of the molecules such as 1,1’-Bicyclopropyl, 2,2,3,’,2’-tetramethyl-, 3-methylpenta-3-yl propyl carbonate, Heptane,4-ethyl-, 1,2-Benzenediol, O-(5- chlorovaleryl)-o’-(1-nephthoyl)-, Acetic anhydride are not known. Further work in this direction is warranted.

Acknowledgements

The authors acknowledge the help received by one and all.

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Author Info

1Department of Physiology, Sree Lakshmi Narayana Medical College and Research Institute, Pondicherry, India
2Department of Anatomy, Sree Balaji Medical College and Hospital, Chennai, Tamil Nadu, India
3M/s. Noahs Laboratories, No, 8/1, Old Mahabalipuram Road, Thiruporur, Tamil Nadu, India
4Department of Anatomy, Chettinad Academy of Research and Education, Tamilnadu, India
5School of Management, Sri Ramachandra Institute of Higher Education and Research, Porur, Chennai, India
6Department Of Anatomy, Vinayaka Mission’s Medical College And Hospital, Karikal, Vinayaka Mission’s Research Foundation, Salem, Tamil Nadu, India
7School of Chemical and Biotechnology, SASTRA Deemed-to-be-University, Thanjavur 613 401, Tamil Nadu, India
 

Citation: Yuvaraj R, Vijayakumar R, Prabhu K, Rao MRK, Balaji TK, Subashree Anantaraman, Kalaivannan J, GAS Chromatography Mass Spectroscopic Analysis Ayyappala Kera Thailam, J Res Med Dent Sci, 2022, 10 (4):78-83.

Received: 30-Mar-2022, Manuscript No. JRMDS-22-58981; , Pre QC No. JRMDS-22-58981 (PQ); Editor assigned: 01-Apr-2022, Pre QC No. JRMDS-22-58981 (PQ); Reviewed: 18-Apr-2022, QC No. JRMDS-22-58981; Revised: 21-Apr-2022, Manuscript No. JRMDS-22-58981 (R); Published: 28-Apr-2022

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