Research Article
Open Access
Development of Analytical Parameters for a
Hepatoprotective Polyherbal Formulation-Liverem
Jayachandra Kuncha1*, P Thirugnanasambantham2, T Muthukumaran3, N Narayanan4, Siva Siddharth5
1Research Scholar, Department of Biotechnology, Periyar Maniammai University, Thanjavur - 613 403, Tamil Nadu, India
2Head, R&D Centre, Rumi Herbals Pvt Ltd., Chennai, India
3Assistant Professor, Department of Biotechnology, Periyar Maniammai University, Thanjavur - 613 403, Tamil Nadu, India
4Director, Department of Pharmaceutics, Jaya college of Pharmacy, Chennai, India
5Director, Rumi Herbals Pvt Ltd., Chennai, India
2Head, R&D Centre, Rumi Herbals Pvt Ltd., Chennai, India
3Assistant Professor, Department of Biotechnology, Periyar Maniammai University, Thanjavur - 613 403, Tamil Nadu, India
4Director, Department of Pharmaceutics, Jaya college of Pharmacy, Chennai, India
5Director, Rumi Herbals Pvt Ltd., Chennai, India
*Corresponding author: Jayachandra Kuncha, Research Scholar, Department of Biotechnology, Periyar Maniammai University, Periyar Nagar, vallam,
Thanjavur - 613 403, Tamil Nadu, India, Tel: +7401486335; E-mail: jayachandrakuncha@gmail.com
Received: August 25, 2015; Accepted: September 14, 2015; Published: September 14, 2015;
Citation: Kuncha J, Thirugnanasambantham P, Muthukumaran T, Narayanan N, Siddharth S (2015) Development of Analytical
Parameters for a Hepatoprotective Polyherbal Formulation-Liverem. SOJ Mater Sci Eng 3(2): 1-7. DOI: http://dx.doi.org/10.15226/sojmse.2015.00125
AbstractTop
Developing analytical parameters for traditional system of
medicines are a crucial step in establishing the quality of herbal
products, presence of phytochemical ingredients and its therapeutic
efficacy. Globally WHO and Nationally AYUSH both specify and
encourage doing quality analysis of herbal raw materials and finished
products which ensure quality and safety. In this research work, a
hepatoprotective polyherbal ayurvedic formulation Liverem has
been taken to establish its quality by using various organoleptic
and physicochemical parameters specified by Ayurvedic and Siddha
pharmacopeias. The results revealed that all the specified parameters
found to be within the limits.
Keywords: Analytical Parameters; Polyherbal Formulation; Hepatoprotective; Physicochemical Parameters
Keywords: Analytical Parameters; Polyherbal Formulation; Hepatoprotective; Physicochemical Parameters
Introduction
The quality control of herbal crude drugs and formulations
is important to justify their acceptability in modern system of
medicine [1]. Polyherbal formulations, which have widespread
acceptability as therapeutic agents include anti-diabetic, lipid
lowering and hepatoprotective agents [2]. Now-a-days, in the
whole world there is turn to return towards the use of herbal
products and to adopt more natural way of life. People prefer
natural food, herbal medicines and natural curing practices for
healthy life. Use of natural remedies for the treatment of liver
diseases has a long history, starting with the ayurvedic treatment
and extending to the Chinese, European and other systems of
traditional medicines. In spite of the tremendous advances made,
no significant and safe hepatoprotective agents are available in
modern therapeutics. Therefore, importance has been given
globally to develop plant based hepatoprotective drugs effective
against a variety of liver disorders [3].
Even though herbal medicines are become popular and effective in the treatment of several ailments, they are still unacceptable in the treatment modalities due to (i) lack of standardization (ii) lack of identification of active ingredient(s) / principle(s) (iii) lack of randomized controlled clinical trials (RCTs) and (iv) Lack of toxicological evaluation. Standardization refers to the body of information and controls, necessary to produce materials of reasonable consistency. This is achieved through minimizing the inherent variation of natural product composition through quality assurance practices applied to agriculture and manufacturing process [4].
Standardization is an important aspect for maintaining and assessing the quality and safety of the polyherbal formulation as combinations of more than one herb to attain the desire therapeutic effect [5]. Standardization minimizes batch to batch variation; assure safety, efficacy, quality and acceptability of the polyherbal formulations [6]. Around globe all countries insisting to do standardization of herbal products by using standard protocols. During this process we can check the quality of product as well as screen the safety parameters such as microbial and heavy metal limit tests, which are play major health concern for the utilization of herbal products.
As a part of research work, a marketed hepatoprotective polyherbal ayurvedic formulation 'Liverem' has been taken to establish its quality by using various organoleptic and physicochemical parameters specified by Ayurvedic [7], Siddha pharmacopeia [8] and WHO [9] guidelines. The herbal ingredients which are used for the formulation has claim that it posses potent hepatoprotective activity. The formulation is manufactured by Rumi Herbals Pvt. Ltd., a GMP certified, and 20 years old company and is marketed by Rohini Global Marketing Pvt Ltd. Chennai.
Even though herbal medicines are become popular and effective in the treatment of several ailments, they are still unacceptable in the treatment modalities due to (i) lack of standardization (ii) lack of identification of active ingredient(s) / principle(s) (iii) lack of randomized controlled clinical trials (RCTs) and (iv) Lack of toxicological evaluation. Standardization refers to the body of information and controls, necessary to produce materials of reasonable consistency. This is achieved through minimizing the inherent variation of natural product composition through quality assurance practices applied to agriculture and manufacturing process [4].
Standardization is an important aspect for maintaining and assessing the quality and safety of the polyherbal formulation as combinations of more than one herb to attain the desire therapeutic effect [5]. Standardization minimizes batch to batch variation; assure safety, efficacy, quality and acceptability of the polyherbal formulations [6]. Around globe all countries insisting to do standardization of herbal products by using standard protocols. During this process we can check the quality of product as well as screen the safety parameters such as microbial and heavy metal limit tests, which are play major health concern for the utilization of herbal products.
As a part of research work, a marketed hepatoprotective polyherbal ayurvedic formulation 'Liverem' has been taken to establish its quality by using various organoleptic and physicochemical parameters specified by Ayurvedic [7], Siddha pharmacopeia [8] and WHO [9] guidelines. The herbal ingredients which are used for the formulation has claim that it posses potent hepatoprotective activity. The formulation is manufactured by Rumi Herbals Pvt. Ltd., a GMP certified, and 20 years old company and is marketed by Rohini Global Marketing Pvt Ltd. Chennai.
Materials and Methods
Plant materials
Phyllanthus amarus (Whole plant), Azadirachta indica
(Leaves), Picrorhiza kurroa (Rhizomes), Eclipta alba (Whole
plant) and Swertia chirayita (Stem and leaves) were procured from local herbal vendors in Chennai with individual quality
control report
Physical examination
All the dry plant materials were examined physically by
spreading in polythene sheet, cleaning was done by experienced
people.
Grinding and sieving
The plant materials were ground into coarse powder with the
help of electric grinder. Sieving was done to get uniform granules
by using sieve No.40.
Raw material quality assessment
The below mentioned parameters were assessed as per the
standards provided by Ayurvedic and Siddha pharmacopeia,
Govt. of India.
Foreign matters: Foreign matter is the material which contain other plant parts, mineral or mud, sand admixtures, products of organism and other than the named material. 100g of the drug sample to be examined was weighed and spread out as a thin layer; the foreign matter was detected by inspection with the unaided eye or by the use of a lens (6x). It was separated, weighed and the percentage of foreign matters present was calculated.
Total ash: The residue remaining after incineration is the ash content of a dry plant material. It is the measure of the total amount of material remaining after incineration. An electric muffle furnace, capable of maintaining a temperature of 625 ± 25 °C was used for measuring ash content.
Foreign matters: Foreign matter is the material which contain other plant parts, mineral or mud, sand admixtures, products of organism and other than the named material. 100g of the drug sample to be examined was weighed and spread out as a thin layer; the foreign matter was detected by inspection with the unaided eye or by the use of a lens (6x). It was separated, weighed and the percentage of foreign matters present was calculated.
Total ash: The residue remaining after incineration is the ash content of a dry plant material. It is the measure of the total amount of material remaining after incineration. An electric muffle furnace, capable of maintaining a temperature of 625 ± 25 °C was used for measuring ash content.
The Ash content (%) = (C - A) / (B - A) X 100.
Where: A = weight of empty crucible (g), B = weight of crucible
and sample (g), C = weight after ashing (g)
Acid insoluble ash: It is the residue obtained after boiling
the total ash with dilute HCl and igniting the remaining insoluble
matter. This measures the amount of silica present, especially
as sand and siliceous earth. The ash obtained was boiled for 5
min with 25 ml of dilute HCl, the insoluble matter was collected
in an ash-less filter paper, washed with hot water and ignited
to constant weight. The percentage of acid-insoluble ash was
calculated.
Water soluble extractive: 5 g of the air dried drug was macerated, coarsely powdered, soak with 100 ml of water in a flask for 24 h, shaking frequently during 6 h and allowed to standing for 18 h. Take 25 ml of the filtrate, evaporated to dryness in a tarred flat bottomed shallow dish and dried at 105°C to constant weight and weighed. The percentage of water-soluble extractive with reference to the air-dried drug was calculated.
Alcohol soluble extractive: 5 g of the air dried drug was macerated, coarsely powdered, soak with 100 ml of Alcohol of the specified strength in a closed flask for 24 h, shaking frequently during 6 h and was allowed to stand for 18 h. Rapidly filtered, taking precautions against loss of solvent, evaporated 25 ml of the filtrate to dryness in a tarred flat bottomed shallow dish, and dry at 105°C, to constant weight and weigh. The percentage of alcohol-soluble extractive with reference to the air-dried drug was calculated.
Loss on Drying or Moisture content: It is the amount of water or volatile content present in the sample. Plant material may get spoiled (microbial attack) if more moisture present. The plant materials were weighed, kept in an oven at 105°C and equilibrated. It was reweighed till three constant readings.
Water soluble extractive: 5 g of the air dried drug was macerated, coarsely powdered, soak with 100 ml of water in a flask for 24 h, shaking frequently during 6 h and allowed to standing for 18 h. Take 25 ml of the filtrate, evaporated to dryness in a tarred flat bottomed shallow dish and dried at 105°C to constant weight and weighed. The percentage of water-soluble extractive with reference to the air-dried drug was calculated.
Alcohol soluble extractive: 5 g of the air dried drug was macerated, coarsely powdered, soak with 100 ml of Alcohol of the specified strength in a closed flask for 24 h, shaking frequently during 6 h and was allowed to stand for 18 h. Rapidly filtered, taking precautions against loss of solvent, evaporated 25 ml of the filtrate to dryness in a tarred flat bottomed shallow dish, and dry at 105°C, to constant weight and weigh. The percentage of alcohol-soluble extractive with reference to the air-dried drug was calculated.
Loss on Drying or Moisture content: It is the amount of water or volatile content present in the sample. Plant material may get spoiled (microbial attack) if more moisture present. The plant materials were weighed, kept in an oven at 105°C and equilibrated. It was reweighed till three constant readings.
Microbial safety profile
All the raw materials must be free from microbial
contamination. It is the major safety parameter to ensure the
product quality. Microbial screening was carried out to estimate
the number of viable microorganism present in the material.
Various differential and selective medias are utilized for screening
microbial contamination. For Total viable count (Casein soya
bean digest agar), Total yeast and moulds (Sabouraud dextrose
agar with antibiotics), E. coli (MacConkey agar and EMB agar),
Salmonella (Brilliant Green agar) Staphylococcus sp. (Mannitol
salt agar) Pseudomonas aeruginosa, (Cetrimide agar) were used
to screen the organisms as per the AYUSH guidelines.
Pre-formulation studies
The below mentioned parameters were assessed as per the
standards provided by Protocols for testing Ayurvedic, Siddha
and Unani Medicines, Dept. of AYUSH, Govt. of India [10].
Organoleptic characters: Texture, Color, Odor and taste were assessed by using sensory organs
pH: Individually, 5% solution was made and the pH was checked by using digital pH meter
Microscopic Characteristics: The powdered materials were spread as thin film on glass slide and observe shape of the granules under the microscope.
Observations under UV light: The materials were mixed with 10% NaOH and 5% HCl and observe under UV light at 254 nm and also observe without adding above constituents.
Flow Properties: Flow properties of drug indicate the uniformity of the granules and it is useful for proper filling and clinical application. The following methods are used to evaluate the flow properties.
Angle of repose: Angle of repose is characteristic related to interparticulate friction or resistance to movement between particles [11]. A funnel was fixed at a particular height on a burette stand. A white paper was placed below the funnel on the table. The powdered drug (5g) passed slowly through the funnel until it forms a pile. The radius of the pile was noted down. Angle of repose of the powder material was calculated by using the formula: tan θ = h/r; θ = tan (h/r) where, h = height of the pile, r = radius.
Bulk density (D0): 25 g of accurately weighed powder was poured into a graduated cylinder, powder bed was made uniform without disturbing the cylinder and the volume was measured directly from the graduation mark on the cylinder as ml [12]. The volume measure was called as bulk volume and bulk density is calculated as Bulk density =
Organoleptic characters: Texture, Color, Odor and taste were assessed by using sensory organs
pH: Individually, 5% solution was made and the pH was checked by using digital pH meter
Microscopic Characteristics: The powdered materials were spread as thin film on glass slide and observe shape of the granules under the microscope.
Observations under UV light: The materials were mixed with 10% NaOH and 5% HCl and observe under UV light at 254 nm and also observe without adding above constituents.
Flow Properties: Flow properties of drug indicate the uniformity of the granules and it is useful for proper filling and clinical application. The following methods are used to evaluate the flow properties.
Angle of repose: Angle of repose is characteristic related to interparticulate friction or resistance to movement between particles [11]. A funnel was fixed at a particular height on a burette stand. A white paper was placed below the funnel on the table. The powdered drug (5g) passed slowly through the funnel until it forms a pile. The radius of the pile was noted down. Angle of repose of the powder material was calculated by using the formula: tan θ = h/r; θ = tan (h/r) where, h = height of the pile, r = radius.
Bulk density (D0): 25 g of accurately weighed powder was poured into a graduated cylinder, powder bed was made uniform without disturbing the cylinder and the volume was measured directly from the graduation mark on the cylinder as ml [12]. The volume measure was called as bulk volume and bulk density is calculated as Bulk density =
Tapped density (Df): After measuring D0, same cylinder was
set to measure tapped density. The cylinder was tapped with 100
tap drop/minute and operated for 500 taps. Volume was noted
as Va, tapping was done again for 750 times and final volume was
noted as Vb. The difference between Va and Vb was calculated and
when it was found to be not more than 2%, then Vb was considered
as final tapped volume and tapped density was calculated using
the following formula =
the following formula =
Compressibility indices: The bulk and tapped densities
were used to calculate the compressibility indices (Carr's index
and Hausner ratio) which provide the flow properties and
compressibility of powders.
The Hausner's ratio is a number that is correlated to the flow ability of a powder or granular material.
Hausner ratio =
The Hausner's ratio is a number that is correlated to the flow ability of a powder or granular material.
Hausner ratio =
Carr's index depends upon the bulk density and tapped
density of a powder and evaluates the rate at which it is packed
down. The following formula was used for the determination of
Carr's Index.
Carr's index =
Carr's index =
Quality control parameters
Composition and Preparation of Capsule: Each 100 mg of
earlier mentioned plant powder materials were mixed properly
by using butterfly mixture and made 500 mg of polyherbal hard
gelatin capsule (Zero size) by using semi automated capsule
filling machine.
Organoleptic characters: Texture, color, odor, taste and uniformity were determined by sensory organs. pH: After preparing 5% solution of the finished product, the pH was checked by using digital pH meter.
Flow properties: For the finished product flow properties like Angle of repose, Bulk density, Tapped density, Carr`s index and Hausner ratio were assessed by standard methods.
Weight variation test: Test for uniformity of weight was performed as per Indian Pharmacopeia (IP), 2007 [13]. Randomly selected 20 capsules were weighed (individually and together) in a single pan balance. The average weight, variation in the individual capsule and the standard deviation was calculated.
Weight variation=
Organoleptic characters: Texture, color, odor, taste and uniformity were determined by sensory organs. pH: After preparing 5% solution of the finished product, the pH was checked by using digital pH meter.
Flow properties: For the finished product flow properties like Angle of repose, Bulk density, Tapped density, Carr`s index and Hausner ratio were assessed by standard methods.
Weight variation test: Test for uniformity of weight was performed as per Indian Pharmacopeia (IP), 2007 [13]. Randomly selected 20 capsules were weighed (individually and together) in a single pan balance. The average weight, variation in the individual capsule and the standard deviation was calculated.
Weight variation=
Drug content uniformity test: Test for drug content
uniformity was carried out as per Indian Pharmacopeia, 2007.
20 capsules were taken and emptied their content in a mortar
and pestle and ground into a fine powder. From this, 500mg
of powder was taken into a volumetric flask and diluted with
phosphate buffer (pH 6.8). The absorbance of the solution was
measured at 213 nm by using UV-Visible spectrophotometer
(Systronics, UV-Vis Spectrophotometer) [14].
Disintegration: This test is useful as a quality assurance tool for conventional dosage forms. The efficacy of a drug can be dependent on the rate at which the capsule disintegrates in the patient's gastrointestinal tract. The disintegration test is a measure of the time required under a given set of conditions for 6 randomly selected capsules to disintegrate into particles which will pass through a 10 mesh screen with in a disintegration assembly at maintained temperature 37±2°C. Disintegration test was performed using the disintegration test apparatus [15].
Disintegration: This test is useful as a quality assurance tool for conventional dosage forms. The efficacy of a drug can be dependent on the rate at which the capsule disintegrates in the patient's gastrointestinal tract. The disintegration test is a measure of the time required under a given set of conditions for 6 randomly selected capsules to disintegrate into particles which will pass through a 10 mesh screen with in a disintegration assembly at maintained temperature 37±2°C. Disintegration test was performed using the disintegration test apparatus [15].
Microbial analysis
Microbial analysis was carried for capsule as per procedures of
Indian Pharmacopeia 2007 and WHO Guideline. The test included
total bacterial count, total yeast and mould count, Identification
of specified organisms such as Escherichia coli, Salmonella sp.,
Staphylococcus aureus and Pseudomonas aeruginosa.
Test for heavy metals
Preparation of samples by acid digestion method:
Accurately weighed 2 g of sample was taken in Kjeldahl flask.
Acid mixture of Nitric acid: Perchloric acid (4:1) was added in the
flask and heated continuously till the solution became colourless.
The sample was then transferred to a 25 ml volumetric flask and
the volume was made-up with distilled water. Reagent blank was
synchronously prepared according to the above procedure. The
standards of Lead, Cadmium, Arsenic and Mercury were prepared
as per the protocol in the manual. The samples were analyzed
for the presence of Pb, Cd, As and Hg using Atomic Absorbance
Spectrophotometer (AAS) (SHIMADZU).
Results and Discussion
Standardization is a system ensuring predefined set of the
quality and therapeutic effect of the constituents in each dose
[16]. Various types of herbal medicines have been used as curative
agents in different parts of the world [17]. Drugs derived from
herbs may have possible therapeutic relevance in the treatment
of illness [18]. The polyherbal formulation was formulated for
hepatoprotective activity by using traditional medicinal plants.
In the earlier research work, the formulation was screened for
hepatoprotective activity in pre-clinical model. The results
showed excellent hepatoprotective activity by CCl4 induced
hepatic damage [19] and also the formulation was prescribed by
Ayurvedic and Siddha Physicians for several liver diseases. In the
present study, Liverem has been taken for the development of
quality control parameters as per Ayurvedic, Siddha, and Indian
Pharmacopeia's, followed by AYUSH and WHO guidelines.
Determination of raw materials Identity and Purity
Selected medicinal plants for formulation were screened
individually for its identity and purity, the given specifications
found within the limits (Table 1). Ash contents were below the
given value which indicates the less contamination. Moisture
content was found to be less than 5% which is a good indicator
for less susceptibility for microbial contamination. Table 1 show
the microbial limits of individual raw material which indicates
within limits. This shows the cleanliness of raw material and
good storage practice in the manufacturing premises.
Pre-formulation studies
Pre-formulation parameters like organoleptic, microscopic,
pH and flow properties such as bulk density, tap density, Carr's
index, Hausner ratio and angle of repose were carried out for the
selected individual raw materials (Table 2).
Quality control parameters for the finished product
In the case of herbal drugs, capsule is the convenient form for
oral administration, better acceptance and reduces esophageal
irritation. The capsule was evaluated by different Pharmacopeial
and non-Pharmacopeial physicochemical tests such as
organoleptic characters, pH, flow properties, weight variation,
moisture analysis, drug content uniformity and disintegration.
3 consecutive batches were tested and the average values were
taken.
The pH of 5% w/v solution was 6.72 which indicate suitability for human use. Other Physicochemical properties of the finished product were also carried out (Table 3). The Indian Pharmacopeia limit for weight variation in case of capsule weighting more than 300 mg is ± 5%. The results showed weight variation of the Liverem capsule found to be within the IP limit. The moisture content was less than 5%, the drug content uniformity also found within IP limit. The disintegration time was found to be an average of 240.16 sec, which means capsule will get disintegrated in the stomach within a short span of time when taken orally. Bulk density, Tapped density, Hausner ratio, Carr`s index and angle of repose were found to be 0.95 g/cm3, 1.03g/cm3, 1.08, 8.07 and 32.83° (Table 4). Value for Carr's index below 15 indicates excellent flowing material and value over 20-30 suggests poor flowing material. Values for angle of repose less than 30ο usually indicates a free flowing material and angle greater than 40ο suggest a poor flowing material [20].
The microbiological and heavy metal profile of the formulation were given in Table 5. The total aerobic, yeast and mould count was 100 cfu/g and 10 cfu/g respectively and Escherichia coli, Salmonella sp., Staphylococcus aureus Pseudomonas aeruginosa were absent in the formulation. Heavy metal contamination is the foremost concern in traditional system of medicine as they are found to be toxic if their level in the body surpasses the respective maximum permitted limits [21].
Among highly toxic environmental pollutants lead is one of the components. When human body exposed to lead it can form complexes with biomolecules and affects neuromuscular, cardiovascular, reproductive and gastrointestinal systems. The organs like liver and kidney severely damaged by lead [22,23]. As per Government of India, AYUSH guidelines permissible limits in Ayurveda, siddha and unani products are less than 10ppm. High levels of cadmium causes damage to the liver and majorly to the kidney due to very slow excretion and it accumulated in this organ and causes irreversible damage to renal tract. It also shows deleterious effect on other organs when exposed to high levels of
The pH of 5% w/v solution was 6.72 which indicate suitability for human use. Other Physicochemical properties of the finished product were also carried out (Table 3). The Indian Pharmacopeia limit for weight variation in case of capsule weighting more than 300 mg is ± 5%. The results showed weight variation of the Liverem capsule found to be within the IP limit. The moisture content was less than 5%, the drug content uniformity also found within IP limit. The disintegration time was found to be an average of 240.16 sec, which means capsule will get disintegrated in the stomach within a short span of time when taken orally. Bulk density, Tapped density, Hausner ratio, Carr`s index and angle of repose were found to be 0.95 g/cm3, 1.03g/cm3, 1.08, 8.07 and 32.83° (Table 4). Value for Carr's index below 15 indicates excellent flowing material and value over 20-30 suggests poor flowing material. Values for angle of repose less than 30ο usually indicates a free flowing material and angle greater than 40ο suggest a poor flowing material [20].
The microbiological and heavy metal profile of the formulation were given in Table 5. The total aerobic, yeast and mould count was 100 cfu/g and 10 cfu/g respectively and Escherichia coli, Salmonella sp., Staphylococcus aureus Pseudomonas aeruginosa were absent in the formulation. Heavy metal contamination is the foremost concern in traditional system of medicine as they are found to be toxic if their level in the body surpasses the respective maximum permitted limits [21].
Among highly toxic environmental pollutants lead is one of the components. When human body exposed to lead it can form complexes with biomolecules and affects neuromuscular, cardiovascular, reproductive and gastrointestinal systems. The organs like liver and kidney severely damaged by lead [22,23]. As per Government of India, AYUSH guidelines permissible limits in Ayurveda, siddha and unani products are less than 10ppm. High levels of cadmium causes damage to the liver and majorly to the kidney due to very slow excretion and it accumulated in this organ and causes irreversible damage to renal tract. It also shows deleterious effect on other organs when exposed to high levels of
Table 1: Individual raw material specifications as per Ayurvedic and Siddha pharmacopeias.
S.No |
Specification |
Phyllanthus amarus |
Picrorhiza kurroa |
Eclipta alba |
Azadirachta indica |
Swertia chirayita |
|||||
API (%) |
Result |
API (%) |
Result |
API (%) |
Result |
API (%) |
Result |
API (%) |
Result |
||
1 |
Foreign matter |
NMT 2 |
0.4 |
NMT 2 |
0.6 |
NMT 2 |
0.5 |
NMT 2 |
0.2 |
NMT 2 |
0.2 |
2 |
Total ash |
NMT 16 |
7.20 |
NMT 7 |
2.80 |
NMT 22 |
5.52 |
NMT 10 |
6.62 |
NMT 6 |
2.24 |
3 |
Acid insoluble ash |
NMT 7 |
2 |
NMT 1 |
0.5 |
NMT11 |
3 |
NMT 1 |
0.6 |
NMT 1 |
0.4 |
4 |
Water soluble Extractive |
NLT 13 |
17.92 |
NLT 20 |
40 |
NLT 15 |
27 |
NLT 19 |
22.5 |
NLT 10 |
12.6 |
5 |
Alcohol soluble Extractive |
NLT 3 |
8 |
NLT 10 |
13 |
NLT 5 |
8 |
NLT 13 |
15.2 |
NLT 10 |
14.3 |
6 |
LOD % |
< 5 |
4.1 |
< 5 |
4.3 |
< 5 |
3.5 |
< 5 |
3.8 |
< 5 |
3.6 |
7.a |
Microbial-TVC (CFU/g) |
1x105 |
110 |
1x105 |
124 |
1x105 |
98 |
1x105 |
85 |
1x105 |
90 |
b |
Total Yeast & Mould (CFU/g) |
1x103 |
10 |
1x103 |
12 |
1x103 |
14 |
1x103 |
11 |
1x103 |
15 |
c |
E. coli |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
d |
Salmonella. sp |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
e |
S. aureus |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
f |
Pseudomonas. sp |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
Absent |
Ab |
NMT – Not more than, NLT – Not less than, API – Ayurvedic Pharmacopeia of India, Ab - Absent
Table 2: Pre-formulation parameters of individual raw materials
S. No |
Specification |
Phyllanthus amarus |
Picrorhiza kurroa |
Eclipta alba |
Azadirachta indica |
Swertia chirayita |
1 |
Texture |
Fine powder |
Fine powder |
Fine powder |
Fine powder |
Fine powder |
2 |
Color |
Light Brown |
Dusty grey |
Dark green |
Greenish |
Light brown |
3 |
Odor |
Indistinct |
Indistinct |
Indistinct |
Indistinct |
Indistinct |
4 |
Taste |
Bitter |
Bitter |
Slightly Bitter |
Bitter |
Bitter |
5 |
pH (5%) |
5.45 |
4.71 |
6.51 |
5.18 |
5.60 |
6 |
Shape |
Fragment cork cells |
Aseptate fibres |
Numerous fibres |
Slender fibres |
Broken fibres |
7 |
Under UV light |
Greenish |
Greenish |
Greenish |
Greenish |
Greenish |
8 |
10%NaOH |
Greenish brown |
Greenish brown |
Greenish brown |
Greenish brown |
Greenish brown |
9 |
5%HCl |
Greenish yellow |
Greenish yellow |
Greenish yellow |
Greenish yellow |
Greenish yellow |
10 |
Angle of Repose |
31.2 |
33.4 |
34.3 |
30.5 |
35.8 |
11 |
Bulk Density (Do) |
0.92 |
0.88 |
0.94 |
0.95 |
0.96 |
12 |
Tap density (Df) |
1.06 |
1.03 |
1.02 |
1.05 |
1.04 |
13 |
Hausner ratio |
1.15 |
1.17 |
1.08 |
1.10 |
1.08 |
14 |
Carr`s index |
13.20 |
14.56 |
7.84 |
9.52 |
7.69 |
Table 3: Organoleptic characters of polyherbal capsule – Liverem.
S.No |
Characteristics |
Batch: 09008 |
Batch: 10009 |
Batch: 11010 |
Average |
1 |
Texture |
Fine powder |
Fine powder |
Fine powder |
Fine powder |
2 |
Color |
Greenish brown |
Greenish brown |
Greenish brown |
Greenish brown |
3 |
Odor |
Indistinct |
Indistinct |
Indistinct |
Indistinct |
4 |
Taste |
Bitter |
Bitter |
Bitter |
Bitter |
5 |
pH (5%) |
6.65 |
6.61 |
6.90 |
6.72 |
6 |
Under UV light |
Greenish brown |
Greenish brown |
Greenish brown |
Greenish brown |
Table 4: Quality control parameters for polyherbal capsule – Liverem.
S. No |
Characteristics |
Batch: 09008 |
Batch: 10009 |
Batch: 11010 |
Average |
1 |
Weight variation |
Within IP limit |
Within IP limit |
Within IP limit |
Within IP limit |
2 |
Moisture analysis % |
3.5 |
3.6 |
4.0 |
3.7 |
3 |
Drug content |
Within IP limit |
Within IP limit |
Within IP limit |
Within IP limit |
4 |
Disintegration (Sec) |
240.11 |
240.16 |
240.22 |
240.16 |
5 |
Angle of Repose (o) |
32.6 |
33.1 |
32.8 |
32.83 |
6 |
Bulk Density(g/cm3) |
0.96 |
0.94 |
0.95 |
0.95 |
7 |
Tap density (g/cm3) |
1.04 |
1.02 |
1.04 |
1.03 |
8 |
Hausner ratio |
1.08 |
1.08 |
1.09 |
1.08 |
9 |
Carr`s index |
7.69 |
7.84 |
8.65 |
8.07 |
cadmium [24 -26]. Limits for cadmium level in ASU products are
less than 0.3ppm.
Arsenic is one of WHO`s ten chemicals of major public health. Arsenic occurs in two forms inorganic and organic. Inorganic arsenic such as arsenic trioxide, arsenic pentoxide and sodium arsenate which is found in water and is highly toxic, while organic arsenic such as monomethylarsonic acid, dimethylarsonic acid and arsenobetamine probably found in sea foods are less harmful to health. Acute effect of arsenic is vomiting, abdominal pain and diarrhoea. Long term effects are skin pigmentation, changes on the palms and soles of feet which also lead to skin, bladder and lung cancers [27]. Permissible limits in ASU products are 03ppm. People generally exposed to methyl mercury through intake of sea foods. Mercury exists in various forms elemental (e.g. methylmercury). These forms of mercury differ in their degree
Arsenic is one of WHO`s ten chemicals of major public health. Arsenic occurs in two forms inorganic and organic. Inorganic arsenic such as arsenic trioxide, arsenic pentoxide and sodium arsenate which is found in water and is highly toxic, while organic arsenic such as monomethylarsonic acid, dimethylarsonic acid and arsenobetamine probably found in sea foods are less harmful to health. Acute effect of arsenic is vomiting, abdominal pain and diarrhoea. Long term effects are skin pigmentation, changes on the palms and soles of feet which also lead to skin, bladder and lung cancers [27]. Permissible limits in ASU products are 03ppm. People generally exposed to methyl mercury through intake of sea foods. Mercury exists in various forms elemental (e.g. methylmercury). These forms of mercury differ in their degree
Table 5: Microbial and Heavy metal analysis of polyherbal capsule – Liverem.
S. No |
Characteristics |
Batch: 09008 |
Batch: 10009 |
Batch: 11010 |
Average |
Microbial limits |
|||||
1 |
Total Bacterial count |
< 100 cfu/g |
< 100 cfu/g |
< 100 cfu/g |
< 100 cfu/g |
2 |
Total Yeast & Mould |
< 10 cfu/g |
< 10 cfu/g |
< 10 cfu/g |
< 10 cfu/g |
3 |
Escherichia coli |
Absent |
Absent |
Absent |
Absent |
4 |
Salmonella sp |
Absent |
Absent |
Absent |
Absent |
5 |
Staphylococcus |
Absent |
Absent |
Absent |
Absent |
6 |
Pseudomonas |
Absent |
Absent |
Absent |
Absent |
Test for Heavy metals |
|||||
A |
Mercury (1 ppm) |
Within limits |
Within limits |
Within limits |
Within limits |
B |
Lead (10 ppm) |
Within limits |
Within limits |
Within limits |
Within limits |
C |
Cadmium (0.3 ppm) |
Within limits |
Within limits |
Within limits |
Within limits |
D |
Arsenic (3 ppm) |
Within limits |
Within limits |
Within limits |
Within limits |
of toxicity and in their effects on nervous, digestive and immune
systems and on lungs, kidney and eyes. 01 ppm is permissible limit
for ASU products. The primary health effect of methylmercury
is impairment of neurological development of foetus. Chronic
exposure to mercury shows cognitive impairment, central and
peripheral nervous system toxicities [28]. The formulation was
checked for the presence of heavy metal contents namely Pb, Cd,
As, Hg and the results are shown in Table 5. None of the heavy
metals was found to exceed their respective permitted level in
the formulation.
Conclusion
Analytical approaches for the polyherbal formulation
standardization is likely to be helpful for quality manufacturing
and supply of herbal drugs to the needy people around the
globe. Conclusively, present study has become a scientific
evidence for the development of quality control parameters and
Liverem-a hepatoprotective polyherbal formulation has passed
all the criteria. Further research on marker compounds analysis,
toxicological studies and clinical trials are in progress.
Acknowledgement
The author expressing thanks to Head, R&D Centre, Rumi
Herbals Pvt Ltd for allowed doing the research work.
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