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Journal of Drug Delivery and Therapeutics

Open Access to Pharmaceutical and Medical Research

Copyright  © 2021 The  Author(s): This is an open-access article distributed under the terms of the CC BY-NC 4.0 which permits unrestricted use, distribution, and reproduction in any medium for non-commercial use provided the original author and source are credited

Open Access  Full Text Article                                                                                                                                         Research Article 

Formulation and Evaluation of Curcumin Gel Sanitizer     

 Roja Maddi1 Surekha Perumalla2 Lalitha Kumari Sesham3 Seema Sultana Shaik4 Jithashma Tanniru5 Hima Bindu Uppu6 Sri Lakshmi Kalasani7, Asiya Begum8*, Rama Rao Nadendla9

1,2,3,4,5,6,7, Students, Department of Pharmaceutics, Chalapathi College of Pharmacy, Guntur, Andhra Pradesh, India

Assistant professor, Department of Pharmaceutics, Chalapathi College of Pharmacy, Guntur, Andhra Pradesh, India

Professor, Department of Pharmaceutics, Chalapathi College of Pharmacy, Guntur, Andhra Pradesh, India

Article Info:

_________________________________________

Article History:

Received 09 June 2021      

Reviewed 21 July 2021

Accepted 28 July 2021  

Published 15 August 2021  

_________________________________________

Cite this article as: 

Maddi R, Perumalla S, Sesham LK, Shaik SS, Tanniru J, Uppu HB, Kalasani SL, Begum A, Nadendla RR, Formulation and Evaluation of Curcumin Gel Sanitizer     , Journal of Drug Delivery and Therapeutics. 2021; 11(4-S):64-70 

DOI: http://dx.doi.org/10.22270/jddt.v11i4-S.4985 

______________________________________________

*Address for Correspondence:  

Asiya Begum, Assistant Professor, Department of Pharmaceutics, Chalapathi College of Pharmacy, Guntur, Andhra Pradesh, India https://orcid.org/0000-0002-7714-6102

Abstract

______________________________________________________________________________________________________

Objective: the main intention of this research is to prepare a curcumin based herbal gel sanitizer by minimizing the alcoholic usage and to evaluate the anti-bacterial activity of this herbal sanitizer. Methods: curcumin gel sanitizer was prepared from the ethanolic extract of Curcuma longa along with addition of gel base prepared from the combination of carbapol-940 and HPMC-E15. Results: The curcumin gel sanitizer was formulated and evaluated for its phytochemical constituents present in curcumin, detection of active constituent of curcumin which was majorly responsible for the anti-microbial activity through HPTLC, organoleptic properties, irritancy test and the efficiency of anti-bacterial activity of curcumin was also evaluated and it is   safe and effective against pathogens. Conclusion: As a natural herb, curcumin which was a household ingredient could also be effectively formulated as a sanitizer that reduces the side effects of alcoholic sanitizer products and is a best source that acts effectively against a numerous pathogens.

Keywords: curcumin, carbapol-940, Ethanolic extract, HPMC-E15 (hydroxypropyl methylcellulose), HPTLC, Pathogens,

 


 

INTRODUCTION

Corona virus is a single-stranded RNA virus with a diameter of about 80–120 nm. It belongs to different genus like α-corona virus, β-corona virus, δ-corona virus and γ – corona virus. SARS-CoV-2 comes under the genus β-corona virus. 4 The emergence of the pandemic COVID-19 has lead to health concern in the public and rapid usage of hand sanitizers is being observed.3 As it can be effective tool of controlling the infection. Recent studies revealed that the transmission of COVID is possible through the mist and the virus can sustain and may become contagious on surfaces about 9 days 2. Hence, it is very important to breakout this conveyance of virus through isolation and by the usage of infection control tools 3. Effective usage of hand sanitizers and face masks could minimize the spread of the virus. According to the analysis of CDC about 2 million people are getting affected by certain infections acquired through the hospitals per year 12. Due to danger imposed by this disease, the CDC of the United States has encouraged and promoted the hand sanitizers usage for the sake of maintenance of hand hygiene12. The availability of Hand disinfectants are in such forms like Non-alcohol based, alcohol-based, herbal sanitizers15.

Hand sanition is a crucial step in controlling the infectious virus in the healthcare systems.9 Numerous hand-sanitation products were accessible outside as they became an emergent rise for the maintanance of hand-hygiene can be seen14. Besides regular soaps, hand sanitizers which consists of different chemical agents with effective anti-microbial properties(such as chlorhexidine, iodophors, quaternary ammonium compounds, triclosan) without the use of water or hand drying materials are used rapidly these days.3

Alcoholic formulations are very effective in various situations. They exterminate various types of pathogens8 but they are not much efficacious in eradicating the organisms such as Clostridium difficile or Bacillus anthracis. In addition rapid usage of these alcohol-based sanitizers can cause flammability, endocrinal disruptions etc.1 Moreover the culture of intentional ingestion of alcohol-containing sanitizers has become popular during this pandemic. 1

 This brings out the case of non-alcohol based sanitizers or herbal based sanitizers which is becoming an option. Medicinal plants consist of abundant secondary metabolites, such as tannins, terpenoids, alkaloids and flavonoids, as these are found to possess greater anti-microbial activity16. Taking this into consideration, the literature screening was performed for different herbs with the anti-microbial properties and founded them (such as Curcuma longa (turmeric), Mentha piperita (peppermint leaves), Eugenia caryophyllus (clove flower buds), and Azadirachta indica (neem leaves)7. Before the discovery of advanced medicine, herbs are the crucial remedy used for various disease treatments. This arrivals of different antibiotics; microbes begin to develop resistance to these antibiotics. This brings the researchers towards the herbs those are abundant in microbial activity.15

This research is carried out by formulating an herbal sanitizer with the extract of Curcuma longa. The ethanolic extract of turmeric has strong anti-microbial properties against the growth of certain microbes such as Pseudomonas aeruginosa, Bacillus cereus and Proteus mirabilis. It also has good anti-fungal activity against Trichophyton longifusus. External application of curcumin was found to decrease variegation and onset of skin tumors.7                                     

 MATERIALS AND METHODS:

 Plant material processing:

Newly harvested rhizomes of curcumin are collected, cleaned and dried under sunlight. The rhizomes after the process of drying were collected and size reduced bypassing through the mesh of suitable size.2

EXTRACTION PROCESS:

Powdered rhizomes of curcumin were extracted with 95% ethanol through the process of maceration for about 24 hours. The obtained crude extract was filtered, concentrated and collected.

PRELIMINARYPHYTOCHEMICAL ASSESSMENT OF CRUDE EXTRACT:

The prepared curcumin extract was assessed for the presence of different phytoconstitutents such as carbohydrates, proteins, alkaloids, flavonoids, tannins and saponins using standard preliminary tests.

CARBOHYDRATES: The curcumin extract is dissolved in 10ml of purified water, filtered and was subjected to the tests for carbohydrates. 17

Molisch test: 2ml of curcumin extract was added into the test tube and few drops of molisch reagent was added to extract. To this 2ml of conc.H2SOwas dropped out from the walls of the test tube. Formation of a violet color ring at the junction of two liquids was observed.17

PROTEINS: The processed curcumin extract was dissolved in 10ml of water, filtered and test for proteins was carried out. 17

 Biuret test: 2ml of filtered solution is treated using a drop of 2% copper sulphate solution. Later on addition of few drops of ethanol (95%). Followed by the addition excess of potassium hydroxide pellets. Pink color formation in ethanolic layer indicates the protein presence. 17

ALKALOID:  the solvent free extract of required17 quantity was added to 3ml of dilute HCL and then filtered. The filtrate was then carried out for the test of alkaloids. 17

Mayer’s test: To 1ml of filtered extract 2 drops of Mayer’s reagent is added from the walls of the test tube. The presence of white or creamy precipitate includes for the alkaloid presence. 17

Wagner’s test: To 1ml of filtrate 2ml of Wagner’s reagent was added from the walls of the test tube.Presence of reddish-brown precipitate confirm positive for the above test.[ 17

Dragendroff’s test: To the 1ml of filtered extract 2ml of Dragendroff’s reagent is added. Formation of yellow color precipitate confirms were positive test17.

GLYCOSIDES

Borntrager’s test:  Prepared curcumin extract was boiled with dilute H2SO4, filtered and the addition of  chloroform was done and shaken well. The separation of organic layer was observed to which ammonia is added slowly. The appearance of pink or red color in ammonical layer indicates positive for the test.13

TERPENOIDS

Salkowski test: To the extract add 2ml of chloroform and 3ml of concentrated H2SO4 was added carefully. A reddish brown color formation indicates presence of terpenoids.13

FLAVONOIDS: To the extract 1.5ml of 50% methanol was slowly added. The  above solution is warmed and magnesium metal was added onto it. To this, addition of concentrated sulphuric acid and red color was observed indicating for  the presence of flavonoids.13

TANNINS: To 0.5ml of extract ,water and few drops of ferric chloride was added. Presence of blue color   indicates for tannins presence.13

SAPONINS: The processed curcumin extract was shaken with 5ml of water and then heated for boil. Frothing shows up for saponins presence. 17

ASSESSMENT OF ISOLATED CURCUMIN BY HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY

EXPERIMENTAL:

Extraction of the curcuminoid from Curcuma longa was carried out with two different solvents and then the isolation of curcumin from the other two components of curcuminoid. 5

Preparation of sample: 0.5gm of Curcuma longa was dissolved in 10ml of ethanol, filtered, concentrated and was collected.

Developing system: Ethyl acetate: n-hexane 3:7 solvent system was made into use for the development of HPTLC fingerprint profile of terpernoids.

 Sample application: Test solution of the curcumin extract(2  and standard solution of the standard curcuminoid extract (3µl) were filled in Hamilton syringe for 5mm band length on percoated silica gel G aluminum plate 60F 254(E MERCK Germany) (3×10cm)  using the applicator connected to AETRON HPTLC system installed and programmed with SPRAYLIN.

 Development of chromatogram: The developed chromatogram was dried at room temperature and then placed in AETRON document chamber and visualized less than 254nm and image of the chromatogram were obtained with an EOS utility, after quantification was done by using the SPRAYLIN software.

FORMULATIONS

Trail No-1

Ethanolic extract of Curcuma longa was prepared by the process of maceration for about 72hours. A gel base was prepared using carbapol and water and transferred into the motor. Filtrate was then added into the motor along with the other ingredients. At last triethanolamine was added and transferred into a bottle.The ingredients were listed in the below table()

Trail No-2

Ethanolic extract of Curcuma longa was prepared by the process of maceration for about 24hrs.The preparation of gel base was achieved by the combination of carbapol-940 and HPMC-E15 in water followed by the addition of NaoH and This gel base was transferred into motor and the herbal extract was added along with the other ingredients and transferred into suitable container. The ingredients were listed in the below table()

Trail No-3  

Herbal extract of Curcuma longa was prepared using ethanol (95%) as a solvent. Gel base was prepared using the combination of Carbapol-940 and HPMC-E15 at the ration of 4:1. The prepared gel base was neutralized using NaoH (10%) which also acts as a cross linking agent. This gel base was transferred to motor and the herbal extract was added one after the other. The remaining ingredients were added onto the motor and then transferred into clear container. The ingredients were listed in the below table().

Table 1: List of ingredients

S.No

Ingredients

Quantity (%)

1.

Curcuma longa

1

2.

Neem oil

q.s

3.

HPMC-E15

0.1

4.

Carbapol-940

0.4

5.

Triethanolamine

1

6.

Glycerin

5

7.

Perfuming agent

q.s

8.

Water

q.s

 

Table 2: List of ingredient

S.No

Ingredients

Quantity Taken (%)

1.

Curcuma longa

2

2.

Neem oil

q.s

3.

Carbapol-940

0.4

4.

HPMC-E15

0.1

5.

NaoH

10

6.

Perfuming agent

q.s

7.

Water

q.s

 

Table 3: List of ingredients

S.No

Ingredients

Quantity (%)

1.

Curcuma longa

5

2.

Neem oil

q.s

3.

Carbapol-940

0.4

4.

HPMC-E15

0.1

5.

NaoH

10

6.

Glycerin

5

7.

Perfuming agent

q.s

8.

Water

q.s

 

 

RESULTS AND DISCUSSION:

RESULTS:

PHTOCHEMICAL SCREENING      

The phytochemical evaluation of ethanolic extract of curcumin results for the existence of secondary metabolites such as carbohydrates, proteins, alkaloids, terpenoids, tannins and flavonoids but the absence of saponins and glycosides. These secondary metabolites serve as competitive weapons against the bacteria, fungi, amoebae and insects.

Table 4: The evaluated phytochemical constituents were listed in the below Table NO-04

S.No

Test

Observation

1.

Carbohydrates

      + Ve

2.

Proteins and amino acids

      +Ve

3.

Alkaloids

      +Ve

4.

Glycosides

       -Ve

5.

Terpenoids

      +Ve

6.

Tannins

      +Ve

7.

Saponins

      -Ve

8.

Flavonoids

     +Ve

 

HIGH PERFORMANCE THIN LAYER CHROMATOGRAPHY OF ISOLATED CURCUMIN

Linear ascending development to a distance of 80mm using the n-hexane and ethyl acetate as mobile phase was carried out in a twin trough glass chamber formerly saturated with the mobile phase vapour for 20min.  Plates were dried in air and photo documented at λ254nm and λ365nm.Results obtained at 365nm were taken out.1

The turmeric (diferuloylmethane) was a polyphenolic compound consists of the active constituents responsible for the anti-bacterial, anti-fungal,anti-oxidant,anti-proliferative activity such as curcumin, bisdemethoxy curcumin, demethoxycurcumin,  curcuminoids e.t.c.

The scan of reference solution revealed the Rf value of 0.68 for the standard and for the test sample it is 0.79. Therefore, the HPTLC evaluation of C.long depicts the presence of the active constituent curcumin in the ethanolic extract of C.longa. 18. The standard reference values for the active constituents of curcumin were provided in the below table-05.

Table 5: The standard reference values for the active constituents of curcumin

S.No

Standard

Rf (cm/cm)

1.

Curcumin

0.69-0.88

2.

Demethoxycurcumin

0.56-0.69

3.

Bisdemethoxycurcumin

0.38-0.56

 

 

 

 

 


 

SAMPLE CURCUMIN

Plate

 


 

 


 

Graph

 

Lanes

ID

Width

Bands

Volume

Notes

1

49

2

16.36

 

Bands

ID

Rf

Area

Volume

Notes

1

0.793

1372

14.2

 

2

0

1127

2.16

 

 

STANDARD CURCUMIN

Plate

image

Graph

image

 

Lanes

ID

Width

Bands

Volume

Notes

1

66

2

3.93

 

 

Bands

ID

Rf

Area

Volume

Notes

1

0.682

2046

0

 

2

0.005

1584

3.93

 

 

 


 

Evaluation Parameters:              

Organoleptic properties: The color, odour and clarity of the formulation were carried out.6

pH: pH of sanitizer was carried out through pH meter and it was observed that the pH of sanitizer was optimum that is exactly 6.9.

Skin Irritant test: Few healthy Volunteers were selected. The formulated curcumin sanitizer was applied on their palm and the time was noted down. Irritancy and itching were checked.11

Evaporation time: Few healthy Volunteers were selected. The curcumin sanitizer was applied on their palm and the time of evaporation was noted down. All the evaluated parameters were provided in the below table-06

Evaluation of anti-bacterial activity: The evaluation of anti-bacterial activity of curcumin gel sanitizer was carried out using different solvents against the strain of aerobic and anaerobic micro-organisms by performing cup-plate method. The nutrient agar medium used for the culture media was provided in the below table-07.

To perform the test, the Petri-plates required for the test must be pre-sterilized to avoid cross-contamination. Petri-plates were pre-sterilized at 1600C in hot air oven. Then, Prepared nutrient agar medium was autoclaved at 1210C   for about 30minutes . Under aseptic conditions culture media was transferred into nutrient agar medium and this entire media is transferred into petri-plate. After, uniform spreading the petriplates were kept aside in until the medium gets solidified.

Table 6:  Composition of nutrient agar medium        

S.No

Ingredients

Quantity(g)

1.

Beef extract

0.2

2.

Yeast extract

0.4

3.

Peptone

1

4.

Sodium chloride

1

5.

Agar

1.5

6.

Distilled water

q.s for 100ml

 

Then, the plates were taken out and cups or wells were made by using cork borer. Then, the standard 95% ethanolic extract of turmeric and the test sample was added into the cup carefully in aseptic conditions. Then both the plates are incubated for 24hrs at 370C.  After, the incubation period, the zone of inhibition was measured on the Petri plate.

The anti-bacterial evaluation of the formulated curcumin gel sanitizer was found to be safe and effective against the bacterial species such as E.coli and Bacillus subtilis. As it can be seen that anti-microbial effect of curcumin sanitier is more efficacious in inhibiting the growth of the microbes as that of the standard i.e ethanolic extract of turmeric. The results were provided in the below table-08.


 

 

 

Table 7: Anti-bacterial evaluation of curcumin gel sanitizer

S.No

Anti-bacterial test

Zone of inhibition(Standard)-mm

Zone of inhibition(Formulation)-mm

1.

E.coli

18

15

2.

B.subtilis

14

11

 


 

Table 8: Evaluation parameters

S.No

Parameter

Formulation

1.

Color

Lemon yellow

2.

Odour

characteristic

3.

pH

6.9

4.

Irritancy test

No irritation

5.

Evaporation rate

20seconds

 

DISCUSSION

The curcumin gel hand sanitizer was evaluated for its phytochemical screening of active constituents, and also the determination of active constituent of curcuma nothing but curcumin through HPTLC and evaluation of organoleptic properties of the formulated herbal gel sanitizer and checked for the irritancy test and the evaporation time. It was found that the above formulation consist of the lemon yellow colour with the gel consistency and smooth texture. It was also tested for its anti-microbial activity against E.coli and B.subtilis and has shown a significant effect against these microbes. The above formulation consists of the ethanolic herbal extract to minimize the alcohol usage in the formulation of the herbal sanitizer.

CONCLUSION

Hands are the common platform for the pathogenic transmission to the people. The proper maintenance of hand hygiene can protect the health from various contagious pathogens especially for the prevention of COVID-19 transmission. WHO recommendation for the usage of alcohol based-sanitizers during this pandemic for the prevention of the disease transmission. But the rapid usage of these alcohol-based sanitizers causing the endocrinal disruptions, flammability and alcohol poisoning if ingested and the intentional ingestion of alcohol containing sanitizers all these were major cases to be considered.

It may be concluded that curcumin gel sanitizer has a significant role as it shows significant effect against specified organisms. Thus, there is immense care in establishing the usage of turmeric gel sanitizer as a measure to control the multi-drug resistant microbes. This herbal gel sanitizer is also based as an alternative for the chemically prepared sanitizers containing active silver nitrates. Natural herbal sanitizers are very efficacious, environmental friendly, and inexpensive.

The above formulation can be use as good sanitizer as the Curcuma longa is much effective against pathogens and its shows effective anti-bacterial activity as a herbal gel sanitizer.

ACKNOWLEDGEMENT

The authors are grateful to the management of chalapathi institute of pharmaceutical sciences for providing all the necessary facilities for the successful completion of the work.

CONFLICT OF INTEREST

The authors declare no conflict of interest.

ABBREVIATIONS

HPMC (hydroxyl propyl methyl cellulose), HPTLC (high performance thin layer chromatography), CDC (centre for disease control and prevention).

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