Physiochemical Analysis of Nilotapaladi Yoga

In Ayurveda many Ayurvedic formulations are explained, which used to treat a variety of illness since ancient time and to protect patient faith in Ayurveda and Ayurvedic treatment, scientifically proven safety, standard and quality of herbs is the need of the hour. Nilotpaladi yoga (NY)  is mentioned in Ayurvedic texts for the Treatment of Raktatisara  (~haemorrhagic diarrohea). Nilotpaladi yoga consists of four ingredients such as Nilakamala (Nymphaea nouchali Burm. f.), Mocharasa (Salmalia malabarica  Schott & Endl.), Lajavanti  (Mimosa pudica  Linn.) and Kamalakesara (Nelumbo nucifera Gaertn.). Nilotpaladi yoga ingredient like Mochrasa (Salmalia malabarica  Schott & Endl.) is known to be effective as Shonita sthapaka gana  (a group of drugs that act as haemostatics). Physiochemical analysis of Nilotpaladi yoga is not explored in detail. So, this article is an attempt to present a physiochemical analysis of ingredients of Nilotpaladi yoga by using Modern analytical Techniques. Physio-chemical analysis, HPTLC etc., were carried out as per standard methods.

A In Ayurveda many Ayurvedic formulations are explained, which used to treat a variety of illness since ancient time and to protect patient faith in Ayurveda and Ayurvedic treatment, scienti ically proven safety, standard and quality of herbs is the need of the hour. Nilotpaladi yoga (NY) is mentioned in Ayurvedic textsfor the Treatment of Raktatisara (~haemorrhagic diarrohea). Nilotpaladi yoga consists of four ingredients such as Nilakamala (Nymphaea nouchali Burm. f.), Mocharasa (Salmalia malabarica Schott & Endl.), Lajavanti (Mimosa pudica Linn.) and Kamalakesara (Nelumbo nucifera Gaertn.). Nilotpaladi yoga ingredient like Mochrasa (Salmalia malabarica Schott & Endl.) is known to be effective as Shonita sthapaka gana (a group of drugs that act as haemostatics). Physiochemical analysis of Nilotpaladi yoga is not explored in detail. So, this article is an attempt to present a physiochemical analysis of ingredients of Nilotpaladi yoga by using Modern analytical Techniques. Physio-chemical analysis, HPTLC etc., were carried out as per standard methods.

MATERIALS AND METHODS
Nilotpaladi yoga (NY) ingredients were purchased from the Gola dinanath market of Varanasi. The identity was con irmed with the help of Sri Dharmasthala Manjunatheshwara centre for research in Ayurveda and Allied Sciences (AYUSH Centre for Excellence and Recognized SIROs by DSIR) Laxminarayana Nagar, P.O. Kuthpady-UDUPI Karnataka. Nilotpaladi yoga ingredients means gum of Salmalia malabarica Schott & Endl., Seeds of Lajavanti (Mimosa pudica Linn.), Stamen of Kamalakesara (Nelumbo nucifera Gaertn.) and petals of Nilakamala (Nymphaea nouchali Burm. f.) were converted into Churna (~powder form). Samples were sent to Sri Dharmasthala Manjunatheshwara Centre for Research in Ayurveda and allied Sciences (AYUSH Centre for Excellence and Recognized SIROs by DSIR). Kuthpady, UDUPI Karnataka, where Physicochemical parameters as depicted in (Table 1) were estimated as per Standard methods described in Ayurvedic Pharmacopeia of India and world health organization standard and HPTLC values were evaluated by using Linomat 5 TLC applicator.

Loss on drying at 105 o C
10 g of each ingredients sample of Nilotpaladi yoga were taken separately in a separate tared evaporating dish. It was then dried at temperature 105°C for 5 hours in the oven and then weighed. The drying continued till the difference between two continuous weights didn't more than 0.01 after cooling by using a desiccator. Moisture percentage calculated in relation to the weight of the sample.

Total Ash
2 g of sample was incarnated in tared platinum crucible at a temperature not exceeding 450°C until carbon-free ash is obtained. The percentage of ash was calculated in relation to the weight of the sample.

Acid insoluble Ash
To the crucible containing total ash, add 25ml of dilute HCl and boil. Collect the insoluble matter on ashless ilter paper (Whatmann 41) and wash with hot water until the iltrate is neutral. Transfer the ilter paper containing the insoluble matter to the original crucible, dry on a hot plate and ignite to constant weight. Allow the residue to cool in a suitable desiccator for 30 mins and weigh without delay. Calculate the content of acid-insoluble ash with reference to the air-dried drug.

Water-soluble ash
Boil the ash for 5 min with 25 ml of water; collect insoluble matter on an ashless ilter paper, wash with hot water, and ignite for 15 min at a temperature not exceeding 450°C. Subtract the weight of the insoluble matter from the weight of the ash; the difference in weight represents the water-soluble ash with reference to the air-dried sample.

Alcohol soluble extractive
Weigh accurately 4 g of the sample in a glass stoppered lask. Add 100 ml of distilled Alcohol (approximately 95%). Shake occasionally for 6 hours. Allow to stand for 18 hours. Filter rapidly, taking care not to lose any solvent. Pipette out 25ml of the iltrate in a pre-weighed 100 ml beaker. Evaporate to dryness on a water bath. Keep it in an air oven at 105 • C for 6 hours, cool in a desiccator for 30 minutes and weigh. Calculate the percentage of Alcohol extractable matter of the sample. Repeat the experiment twice, and take the average value.

HPTLC
1g of each of Nilakamala, Mocharasa, Lajavanti, Kamalakesara and Churna formulation (1part of each of the ingredient) was extracted with 10 ml of alcohol. 5µl of each of the above extract was applied on a pre-coated silica gel F254 on aluminum plates to a band width of 7 mm using Linomat 5 TLC applicator. The plate was developed in Toluene: Ethyl Acetate (9.0: 1.0). The developed plates were visualized in under short UV, long UV and then derivatised with vanillin sulphuric acid and scanned under UV 254nm, 366nm and 620nm (the following derivatisation). Rf, colour of the spots and densitometric scan were recorded (Tables 2, 3 and 4) and Figures 1  and 2 a-d, Figure 3 a-d & Figure 4 a-d).

RESULTS AND DISCUSSION
Physiochemical analysis is an important tool to ind out the quality, standard and ef icacy of Ayurvedic drugs and by correct identi ication, it can be helpful in preventing adulteration (Srikanth et al., 2019). Ash values used to be an important tool to assess the purity of herbs. The Ash and extractive values is the fastest means of determining the quality and ef icacy of Herbs. Acid insoluble ash is a part of total ash and tells us the amount of siliceous earth (Srikanth et al., 2019). Physiological Parameters evaluation of Nilotpaladi yoga is depicted in (Table 1). Loss of drying was maximum seen in Mocharasa (Salmalia malabarica Schott & Endl.) (10.97%) and minimum in Lajavanti (Mimosa pudica Linn.) (6.77%). Total ash values maximum Nilakamala (Nymphaea nouchal i Burm. f.) (10.83) and minimum Lajavanti (Mimosa pudica Linn.) (5.44%). Each Nilotpaladi yoga ingredients Standardization Parameters Results depicted in (Table 1).
With HPTLC, authentication of many types of plant possible, as well as the analysis of stability and con-        (Dhalwal et al., 2008). HPTLC Fingerprinting, by examining R f values and color of the spots, is one of the easiest pharmacopeial parameters to evaluate the qualitative compositional characteristics of any crude drug extracts. HPTLC of ethanolic extract of Nilotpaladi Yoga TLC photo documentation con irmed the detection of various photoconstituents with separate R f values (Figure 1,  Tables 2, 3 and 4). HPTLC photo documentation of Alcoholic fraction of Nilakamala, Mocharasa, Lajavanti, Kamalakesara Churna (Figure 1), under Short UV and After derivatization showed no any spots ( Figure 1). Therefore, R f Value at short UV and after dervivatization can not be observed (Figure 1, Tables 2 and 4 Table 3).
Out of 3 peaks seen on densitometric scan at 254nm, compounds with R f 0.03 (78.31%) was the major peaks (Figure 2 a); at 366, out of 9 peaks, peak with R f 0.67 (41.26%) was the major peak detected (Figure 3 a); at 620nm, out of 10 peaks, peak with R f 0.08 (34.09%) was the major peak seen (Figure 4  Out of 3 peaks seen on densitometric scan at 254nm, compounds with R f 0.03 (92.92%) was the major peaks (Figure 2 b); at 366, out of 8 peaks, peak with R f 0.66 (37.26%) was the major peak detected (Figure 3 b); at 620nm, out of 5 peaks, peak with R f 0.05 (89.80%) was the major peak seen (Figure 4 b). Lajavanti (Mimosa pudica Linn.) on densitometric scan of the plates, 9, 3 and 5 bands were detected under 254nm, 366nm and 620nm, respectively (Figure 2 c, Figure 3 c & Figure 4 c). Out of 3 peaks seen on densitometric scan at 254nm, com-pounds with R f 0.04 (52.85%) was the major peaks (Figure 2 c); at 366, out of 3 peaks, peak with R f 0.66 (57.64%) was the major peak detected (Figure 3 c); at 620nm, out of 5 peaks, peak with R f 0.07 (34.05%) was the major peak seen (Figure 4 c). Kamalakesara (Nelumbo nucifera Gaertn.) on a densitometric scan of the plates, 4, 5 and 7 bands were detected under 254nm, 366nm and 620nm, respectively (Figure 2 d, Figure 3 d & Figure 4 d). Out of 4 peaks seen on densitometric scan at 254nm, compounds with R f 0.04 (64.48%) was the major peaks (Figure 2 d); at 366, out of 5 peaks, peak with R f 0.65 (60.34%) was the major peak detected (Figure 3 d); at 620nm, out of 7 peaks, peak with R f 0.04 (39.10%) was the major peak seen Figure 4 d).
These ingerprints will be helpful to serve the purpose of evaluation of the identity of chemical composition qualitatively.

CONCLUSION
The results and the standards used in Physiochemical analysis and HPTLC indings of Nilotpaladi Yoga ingredients surely be useful as an important part for validation and quality checking of crude drugs used in NY. This study may be useful for Researches etc. As this article is only dealt with Physio-chemical analysis, the implementation and outcome of this Nilotpaladi Yoga will be published separately.