Physicochemical Analysis of Alocasia sanderiana W. Bull
P. Selvakumar1*, Devi Kaniakumari2,
V. Loganathan1
1Department of Chemistry, Periyar
University, Salem, Tamilnadu, India.
2Department of Chemistry, Quaid-E-Millath Govt. College for Women, Chennai, India.
*Corresponding Author E-mail: chemistry.engg@gmail.com
ABSTRACT:
The present investigation reveals standardization
which includes moisture content, total ash, acid insoluble ash, water soluble
extractive value and loss on drying of Alocasia sanderiana W.Bull ethanolic
leaf, stem and root tuber extracts. Total ash value
is useful in determining authenticity and purity of drug and also these values
are important quantitative standards. Total ash value
of plant material indicated the amount of minerals, and earthy materials
present in the plant material. Analytical results showed the total ash higher
value was 3.30% w/w in ethanolic root tuber extract of Alocasia sanderiana. Percent weight loss on
drying or moisture content of ethanolic leaf, stem and root tubers extracts is
63.69%, 73.35% and 75.63%. The less value of moisture content could prevent
bacterial, fungal or yeast growth. Leaf ethanolic extracts having less value
compared stem and root tuber extracts. Ethanolic leaf extracts shows more
antimicrobial activity. The higher amount of acid-insoluble siliceous matter
present in the tuber extracts of A. sanderiana was 0.95w/w%. The water-soluble extractive
value indicated the presence of sugar, acids, and inorganic compounds. The
ethanolic root tuber extract have higher value of water soluble extractive
values.
KEYWORDS:
Total Ash Value, Acid
insoluble ash, Water insoluble ash, Water soluble extractive, Loss on drying, Physico-Chemical Analysis, Alocasia sanderiana.
1. INTRODUCTION:
Alocasia sanderiana W.Bull
is a plant in the Araceae family. Alocasia
sanderiana W.
Bull is also known as the kris plant because of
the resemblance of its leaf edges to the wavy blade of the kalis
dagger (also known as kris plant). It is a tropical
perennial with upright shiny, V-shaped and deeply lobed leaves. The plant can
be up to 6 ft (2m) tall and large in its native habitat. However, cultivated
specimens are smaller. It possesses leaves that are evergreen, pelted,
V-shaped, deeply lobed, and a glossy deep-green with large silvery white veins.
They are about 12-16 in (30-40cm) long and 6-8 in (15-20cm) wide, with
red-green undersides. The leaf stem is about 2 ft (60cm) long.
The rhizome of A. Sanderiana is vertically placed and is known as root
stock. Female flowers are grouped at the lower part of the inflorescence,
whereas the male flowers are at the top. According to literature report, alocasia is a kris plant native
to tropical and subtropical Asia to Eastern
Australia. Alocasia
genus consists of about 79 species of which 28 are cultivated variety. Alocasia sanderiana W. Bull
plant extract used in nanosilver particles to fight
and prevent bacteria in vitro[1] and Alocasia sanderiana W. Bull endemic plant available in Tamilnadu[2,3,4], India[5]. The various species of alocasia plats are used in the treatment of dysentery and
leucorrhoea and they have anti-inflammatory, wound healing[6], cytotoxic [7,8,9], antimicrobial [10-14], Antioxidant [15-19],
antidiabetic [20,21], anticancer [22] and antitumor
properties [23-25]. This plant my previous study shows antimicrobial,
antioxidant, anti-inflammatory, antidiabetic activity
of different parts like leaf, stem, and root tubers ethanolic extracts of Alocasia sanderiana W.Bull plant.
The aim of the present study is to evaluate the physico-chemical
analysis [26, 27] of different parts like leaf, stem, and root tubers of Alocasia sanderiana W.
Bull plant ethanolic extracts.
2. MATERIALS AND METHODS:
2.1.
Materials:
All
chemicals and solvents are of analytical reagent grade and procured from HI
MEDIA and SD FINE chemicals. The healthy and disease free plant parts leaf,
stem and root tubers of Alocasia sanderiana were collected from southern region of
Coimbatore, Tamilnadu, India, in the month of January
2012. The botanical identification was authenticated by a botanist. The fresh
plant parts of each leaf, stem and root were washed with tap water and then
rinsed with distilled water. Washed plant material was air dried in the
laboratory at room temperature for 5-8 days or until they were easily broken by
hand. Once completely dried, plant parts were grounded to a fine powder using
an electronic blender. Plants were stored in a closed container at room
temperature until required.
2.2.
Preparation of ethanolic crude extract:
The
powdered plant parts leaf, stem and root of each material were mixed with
sufficient quantity of ethanol solvent. It was kept in rotary shaker at 100rpm
for 48 hrs. At the end of 48 hrs, each extract was filtered through Whatman
No.1 filter paper and the filtrates were concentrated at room temperature in
order to reduce the volume. The paste like extracts were stored in pre-weighed
screw capped bottles and the yield of extracts were weighed. These screw capped
bottles were kept in refrigerator at 4°C for future use. Each extract was
individually reconstituted using minimal amounts of the extracting solvent
prior to use.
3. Physicochemical studies:
3.1. Determination of Total Ash Value:
Weigh
an empty silica crucible along with lid, previously ignited for one hour.
Transfer 1 gm of sample into the crucible and cover the crucible with lid and
again weigh it. Ignite the crucible for 3 hrs around 4500C
temperature. Ignite for successive
one-hour periods where ignition to constant weight is indicated. Upon the
completion of each ignition, cover the crucible and allow it to cool in a desicator to room temperature before weighing.
Residue wt
Ash
Value = _______________ x 100
Sample
wt
3.2. Determination of Acid
insoluble Ash Content:
Ash obtained from the
total ash was boiled with 25ml of 2N HCl for a few
minutes. Filtered through an ash less filter paper. The filter paper was transferred into a
tarred silica crucible. Incinerated at
450°C in a muffle furnace until free from carbon. The crucible was cooled and
weighed. Percentage of acid insoluble ash was calculated.
3.3. Determination of Water insoluble ash:
Ash obtained from the total ash was boiled with 25 ml
of distilled water for a few minutes and filtered through an ash less filter
paper. The filter paper was transferred into a tarred silica crucible. Incinerated at 450°C in a muffle furnace
until free from carbon. The crucible was cooled and weighed. Percentage of
water-soluble ash was calculated.
3.4. Determination of Water soluble extractive value:
About 1gm of air-dried extracts was taken with 100 ml
of chloroform water in a closed flask for 24 hrs shaking frequently during the
first 6 hrs and then allowed to stand for 18 hrs. Thereafter, it was filtered
rapidly taking precautions against loss of the water. The 25mL filtrate was
evaporated to dryness in a tarred flat bottomed shallow dish, dried at 105°C
weighed. The percentage of the water
soluble extractive value was calculated.
3.5. Determination of Moisture
Content:
1 g of each sample were placed in
pre-weighed flat porcelain dish, dry in the oven at 100o C ±5◦C
till the constant weight was obtained. The loss of weight was calculated.
Weight loss
Moisture Content = _______________x 100
Sample wt
Physicochemical
studies like total ash, acid insoluble ash, water insoluble ash, water soluble extractive
value and loss on drying
at 105°C were carried out as per the WHO guidelines for individual leaf, stem
and root tubers extract of Alocasia sanderiana values are recorded in the Table 1.
Table. 1 Physico-Chemical
Parameters of ethanolic extracts of Alocasia
sanderiana W.Bull
S.No |
Test Parameters |
Leaf
extract % |
Stem
extract % |
Root
tuber extract % |
1 |
Odour |
Pleasant |
Pleasant |
Pleasant |
2 |
Total Ash
Value (w/w %) |
2.23 |
2.97 |
3.30 |
3 |
Acid
insoluble ash (w/w %) |
0.77 |
0.91 |
0.95 |
4 |
Water insoluble ash (w/w
%) |
1.71 |
1.62 |
1.85 |
5 |
Water soluble extractive
(w/w %) |
17.11 |
18.22 |
22.97 |
6 |
Loss on drying (w/w %) |
63.69 |
73.35 |
75.63 |
4.
RESULTS AND DISCUSSION
Physico-Chemical
parameters:
Results of quantitative analysis for total ash, acid
insoluble ash, water insoluble ash, water soluble extractive, loss on drying at
105ºC values are tabulated in Table 1. Total ash
value is useful in determining authenticity and purity of drug and also these
values are important quantitative standards. Total ash
value of leaf, stem and root tuber value of 2.23, 2.97 and 3.30%. Total Ash
value of plant material indicated the amount of minerals, and earthy materials
present in the plant material. Analytical results showed the total ash higher
value was 3.30% w/w in ethanolic root tuber extract of Alocasia sanderiana.
Percent weight loss on drying or moisture content of
ethanolic leaf, stem and root tubers extracts is 63.69, 73.35 and 75.63%. The
less value of moisture content could prevent bacterial, fungal or yeast growth.
Leaf ethanolic extracts having less value compared stem and root tuber
extracts. The higher amount of acid-insoluble siliceous matter present in the tuber extracts of
A. Sanderiana was 0.95% w/w. The
water-soluble extractive value indicated the presence of sugar, acids, and
inorganic compounds. The ethanolic root tuber extract have higher value of
water soluble extractive values.
5.
CONCLUSION
Total ash value is useful in
determining authenticity and purity of drug and also these values are important
quantitative standards. Total ash value of plant
material indicated the amount of minerals, and earthy materials present in the
plant material. Analytical results showed the total ash higher value was 3.30%
w/w in ethanolic root tuber extract of Alocasia sanderiana. Percent weight loss on drying or
moisture content of ethanolic leaf, stem and root tubers extracts is 63.69%,
73.35% and 75.63%. The less value of
moisture content could prevent bacterial, fungal or yeast growth. Leaf
ethanolic extracts having less value compared stem and root tuber extracts.
Ethanolic leaf extracts shows more antimicrobial activity. The higher amount of
acid-insoluble siliceous matter present in the tuber extracts of
A. Sanderiana was 0.95 w/w%. The
water-soluble extractive value indicated the presence of sugar, acids, and
inorganic compounds. The ethanolic root tuber extract have higher value of
water soluble extractive values. From the ethanolic extracts of A. Sanderiana, two new compounds have been isolated. The
characterization and structural conformation of the new compounds are in
progress.
6.
REFERENCES:
1.
Elżbieta Zenkteler, Piotr Sobiczewski, Teresa Orlikowska, Krzysztof Langer, Jerzy
Langer. Application of nanomaterials to fight and
prevent bacteria in vitro. Acta Biologica
Cracoviensia Series Botanica.
Vol. 51, suppl. 1, 2009, 28.
2.
Thankappan Sarasabai, Shynin Brintha, James Edwin James
and Solomon Jeeva. Vascular Plants, Scott Christian
College, Nagercoil, Tamilnadu,
India. Science Research Reporter, 2015, 5(1):36-66.
3.
WikimediaCommons(2016),
https://commons.wikimedia.org/wiki/Category:Cultivated_Plants of_Yercaud, Accessed on 23th February 2016
4.
Thangavelu Muthukumar, Eswaranpillai
Uma, Perumalsamy Priyadharsini. Occurrence of foliicolous
parasitic alga Cephaleuros virescens
on cultivated ornamental plants in southern India, Botanica
Lithuanica, 2014, 20(2): 87–98.
5.
Arvind Singh, Observations on the Flora of Varanasi District in Uttar Pradesh
State of India, Global Journal of Environmental Science and Technology. Vol. 3(10):
pp 368-389, 2015.
6.
Santosh Kumar Singh, Sonia
Thakur, Neha Shukla, Sanju Singh. Wound healing activity of Alocasia macrorrhizos (l.) G.don plant-an
experimental study. Global J Res. Med.
Plants and Indigen. Med. 3, 10, 381-388, 2014.
7.
Rahman M, Hossain A, Siddique SA, Biplab KP, Uddin H. Antihyperglycemic, antioxidant, and cytotoxic
activities of Alocasia macrorrhizos
(L.) rhizome extract. Turk J Biol 36 (2012) 574-57.
8.
Omale James, Okafor Oolycarp Nnacheta and Omede Ameh. Polyphenol contents, cytotoxicity and antioxidant activities of some selected nigerian vegetable foods. Int. J. Chem. Sci.:
6(4),1714-1725, 2008.
9.
Haque M, Jahan T, Rashid MA. Antibacterial and Cytotoxic
Activities of Alocasia fornicata (Roxb.). Int J Nutr
Pharmacol Neurol Dis.
2014;4, S1:29-33.
10.
Wang H X., Ng T.B.(2003). Alocasin,
an antifungal protein from rhizomes of Alocasia macrorrhiza. Protein expression and purification;
28(1):9-14.
11.
Mulla WA, Sargade PB, Pawar AM, Tarkasband HA, Sayyad FJ, (2010).
Evaluation of antimicrobial activity of leaves of Alocasia indica Linn. International Journal of Pharm Tech Research; 2(1): 327-333.
12.
Hoque T, Sikder MA, Kaisar MA, Asad A, Chowdhury, Rashid MA,
(2011) Biological Screenings of Two Araceous Plants
Growing in Bangladesh. Dhaka Univ. J. Pharm. Sci;10(2):131-35.
13.
Haque M, Jahan T, Rashid MA. Antibacterial and Cytotoxic
Activities of Alocasia fornicata (Roxb.). Int J Nutr
Pharmacol Neurol Dis. 2014;
4, S1:29-33.
14.
Judee N. Nogodula, Jessa Marie D. Draug, Maryjane S. Jamero, Charmaine Lei E. Suyom. Phytochemical and Antibacterial Action of Taro (Colocasia esculenta, Araceaea) Aqueous-Ethanolic Leaf Extract against Selected
Bacterial Strains. UIC Research Journal.2012.18(1):221-236.
15.
Mulla WA, Kuchekar SB, Thorat VS, Chopde AR, Kuchekar BS, (2010).
Antioxidant, Antinociceptive and anti-inflammatory
activities of ethanolic extract of leaves of Alocasia indica Schott. Journal of young
pharmacist;2(2):137-143.
16.
Rahman M, Hossain A, Siddique SA, Biplab KP, Uddin H. Antihyperglycemic, antioxidant, and cytotoxic
activities of Alocasia macrorrhizos
(L.) rhizome extract. Turk J Biol 36 (2012) 574-57.
17.
Suman Khowala, Swagata Pal, Ankita Bhattacharjee, Sandip Mukherjee, Koushik Bhattacharya. Antioxidant and Hepatoprotective
Activity of Ethanolic Extract of Alocasia indica Tuber. American Journal of Phytomedicine
and Clinical Therapeutics -AJPCT. 2: 2: 2014;191-208.
18.
Gouriprosad Data, Subhashree Basu, Anurupa Sen, Moumita
Das and Pranabes Nath. Phytochemical evaluation and in vitro study of antioxidant potency of
Amorphophallus campanulatus,
Alocasia indica and Colocasia esculenta: A Comparative
Analysis. Int J Pharm Bio Sci 2012, 3(3): (P) 170-180.
19.
Saswati Roy, M. Dutta Choudhury, S.B. Paul.
Antioxidant potential of rhizome of Alocasia decipiens schott. Asian J Pharm Clin Res, Vol 6, Issue 2, 2013, 120-122.
20.
Md. Rabiul Karim, Nasrin Ferdous,
Narayan Roy, Subed Chandra
Dev Sharma, M. G. Sarowar Jahan,
Mohammad Shariar Shovon. A
study on antidiabetic activity of the leaf and stem
of Alocasia indica L. in steptozotocin induced diabetic rats. International Journal
of Biosciences . 5, 6, 195-202, 2014.
21.
S. A. Sreenivas, P. V. Deshmukh, M. Srikanth, Avijit Choudhury, A. E. Wagh. Antidiabetic and Hypolipidemic Potential of Alocasia
indica Schott. Leaves in Streptozotocin
Induced Diabetic Rats. Int. J. Drug Dev. and Res., 2012, 4 (4): 368-374.
22.
Shengtao Fang, Caiyu Lin, Quanbo Zhang, Li Wang,
Ping Lin, Jie Zhang, Xiujie
Wang. Anticancer potential of aqueous extract of Alocasia macrorrhiza against hepatic cancer in vitro and in vivo. Journal of Ethnopharmacology, 141, 3,
2012, 947-956.
23.
Lei Xiao, Feng Yi, Liang Shuang, Zheng Xiang-Wei. Chemical
Components of the Tuber of Alocasia cucullata. Chemistry of Natural Compounds. 2014, 50(1)
133-134.
24.
Wei P, Zhiyu C, Xu T, Xiangwei Z. Antitumor
effect and apoptosis induction of Alocasia cucullata (Lour.) G. Don in human gastric cancer cells in vitro and in vivo. BMC Complement Altern Med. 2015 ,15:33.
25.
Peng Q, Cai H, Sun X, Li X, Mo Z, et al. (2013) Alocasia cucullata Exhibits Strong Antitumor Effect
In Vivo by Activating Antitumor Immunity. PLoS ONE
8(9): e75328, 2013.
26.
Tasneef Ahmad, Swatantra Bahadur Singh, Shivshankar Pandey. Phytochemical
Screening and Physicochemical Parameters of Crude Drugs: A Brief Review.
International Journal of Pharma Research and Review,
Dec 2013; 2(12):53-60.
27. Bhawana Pandey, Divya Gangrale,
Nikita Upadhyay and Priyanka
Tiwari. Chemical analysis of Pterocarpus santalinus L. extracts. Indian J. Sci. Res.4
(1):201-204, 2014.
Received on 23.02.2016 Accepted on 15.03.2016
© Asian Pharma
Press All Right Reserved
Asian J. Pharm.
Ana. 6(1): January-
March, 2016; Page 31-34
DOI: 10.5958/2231-5675.2016.00005.3