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Original Article
Year :  |  Volume : 7   |  Issue :1   |  Page :25-27  

Thilaga Thendral, T. Lakshmi

Correspondence Address:Department of Pharmacology, Saveetha Dental College and Hospitals, Saveetha University, Chennai, Tamil Nadu, India

Source of Support: None , Conflict of Interest: None

DOI: 10.4103/2231-4040.197331

How to cite this article:

Thendral T, Lakshmi T. Antifungal activity of Acacia catechu bark extract against dermatophytes: An in vitro study. J Adv Pharm Edu Res 2017;7(1):25-27.

  Introduction   Top

Dermatophytes are a group of filamentous fungi that cause infections of the skin. Diseases caused by dermatophytes include athlete’s foot, ringworm, and nail infections. Dermatophyte infections in immune compromised patients can be quite severe.[1,2] Dermatophytes are fungi that require keratin for growth. The organisms colonize the keratin tissues and inflammation is caused by host response to metabolic byproducts.[3-5] These infections are long lasting and are difficult to treat.[6]

The incidence of dermatophytic infections has increased in the past decades. Dermatophytes are responsible for serious human pathogenic disorders in various parts of the world. The incidence of these infections are more in tropical countries, their humid climate, population, and poor hygiene make an ideal condition for the growth of these organisms. Although control measures are available, they have limited effectiveness. Conventional antifungal agents such as chlorhexidine and imidazole derivatives have limited uses. Due to their common side effects such as hepatotoxicity, nausea, diarrhea and impotency, the use is restricted in pregnant and the young people.[7-9]

Dermatophytic infections can be treated either topically or systemically; the method chosen will depend on the type of infection, the severity of the infection, and the patient’s preferences.[10]

Acacia catechu commonly known as karungali in Tamil and khadira in Sanskrit is an evergreen tree with lots of nutritional and medicinal value. People in Kerala consume karungali water for relieving digestive disorders.[11-15] It exhibits diverse pharmacological effects such as antibacterial, antioxidant, hepatoproective, anti-inflammatory, antiviral, analgesic, antipyretic, antiulcer, anticancer activity. The phytochemical constituents such as epigallocatechin, epicatechin, rutin, quercetin present in it produces antibacterial and antioxidant effects.[16-22]

Keeping this in view, this study was designed to evaluate the in vitro anti-dermatophytic activity of Ficus racemosa against Microsporum gypseum, Trichophyton rubrum, and Epidermophyton floccosum. 

  Materials and methods   Top

Plant material

A. catechu willd. bark (AAE/9007) was collected from Hosur, Tamil Nadu, and was authenticated by Dr. H. B. Singh, raw materials herbarium and museum, NISCAIR, NewDelhi. The voucher specimen is preserved for further use in Green Chem Lab, Bengaluru.

Ethanolic extraction

Barks were shade dried for a week. Dried barks were milled to fine powder. Powder was passed through 100 mesh sieve and stored in a sealed polythene bag. 2.5 kg of powdered A. catechu bark were extracted with 10 L of ethanol, at 65°C temperature, for 1 h, in a 20 L round bottom flask with Graham condenser attached. Condenser  was cooled circulating with chilled water. After 1 h of extraction, round bottom flask was cooled to room temp and the extract was filtered and collected. The Marc was extracted repeatedly with 10 L of ethanol, twice. The extracts were filtered and collected. The combined extracts were evaporated to dryness under reduced pressure in a Buchi Rotary Evaporator (Switzerland) at 65°C, to obtain 150 g of powder extract. The w/w yield of the prepared extract was 6%. The extract was stored at 4°C until used.

Fungal cultures

Three fungal pathogens used were procured from the Institute of Microbial Type Culture Collection (MTCC), Chandigarh, viz., M. gypseum MTCC No. 2819, T. rubrum MTCC No. 296, and E. floccosum MTCC No. 613 and are maintained in Sabouraud dextrose agar.

Antifungal activity

Well diffusion method

On sterile plates containing Sabouraud dextrose agar, the fungal cultures were swabbed. Wells of 6 mm diameter were bored in each plate. The wells were filled with varying concentrations of the sample. The plates were incubated at 28°C for 72 h for evaluation. The diameter of inhibition zones formed around the wells was measured in millimeter. The study was performed in duplicates for all the samples.[23]

  Results   Top

Discussion   Top

Conclusion   Top

References   Top




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