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Vol.11 No.4

Arshiya Sultana(Department of Ilmul Qabalat wa Amraze Niswan (Obstetrics and Gynecology), National Institute of Unani Medicine) ; Aynul Fazmiya Mohamed Joonus(Department of Ilmul Qabalat wa Amraze Niswan (Obstetrics and Gynecology), National Institute of Unani Medicine) ; Khaleequr Rahman(Dept. of Ilmul Saidla, National Institute of Unani Medicine) pp.17-17 https://doi.org/10.5667/CellMed.2021.0017
초록보기
Abstract

Episiotomy is the commonest obstetrics intervention in the world to reduce severe perineal injuries. Its prevalence is 43% to 100% in primiparous women in Asia. Further, worldwide approximately 10-95% of pregnant women undergo episiotomy incision during birth. Delay in wound healing probably increases the risk of wound infection, changes the muscular structure, and ultimately causes muscle tone loss. So, wound care is of specific significance to postnatal maternal outcomes. Hence, this case study aimed to evaluate the effect of Marham-i-Raal in episiotomy wound healing and pain relief. The study was conducted in eleven postpartum primi or multipara pregnant women aged between group 19 and 35 years with term gestational age, singleton pregnancy in a cephalic presentation who had a normal vaginal delivery with mediolateral episiotomy, without a perineal tear, and perineal hematoma. Externally, application of Marham-i-Raal 2g on episiotomy incisional wound, twice a day for 10 days was advised. Wound healing of episiotomy and pain intensity was assessed with REEDA [“redness, oedema, ecchymosis, discharge and approximation of the edges”] scoring and VAS scoring for pain intensity respectively. At one hour (baseline), the REEDA mean score of eleven patients was 3.90±1.04 whereas on day 7-10 it was 0.18±0.40 with statistically significant difference (p<0.001). The VAS mean score at one hour was 6.90±1.22 whereas on day 7- 10 it was 0.72±0.78 with a statistically significant difference (p <0.001). Marham-i-Raal would be effective in episiotomy wound healing and reducing pain intensity. Further, randomized double-blind controlled trials in large sample size are recommended.

Shahnawaz(Dept. of Ilmul Saidla, National Institute of Unani Medicine) ; Khaleequr Rahman(Dept. of Ilmul Saidla, National Institute of Unani Medicine) ; Arshiya Sultana(Dept. of Amraze Niswan wa Ilmul Qabalat, National Institute of Unani Medicine) ; Shabiya Sultana(Dept. of Tahaffuzi wa Samaj Tib, National Institute of Unani Medicine) pp.18-18 https://doi.org/10.5667/CellMed.2021.0018
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Abstract

Jawarishe Jalinoos (JJ) is an orally used formulation available in semisolid dosage form, prepared with powdered plant materials mixed in honey or sugar syrup. It has many admirable pharmacological effects and used in Unani medicine to treat various acute and chronic disorders since ancient times. The ICH Harmonised Tripartite Guideline stated that photostability testing should be an essential part of stability testing to confirm that light exposure does not result in an unacceptable change in drugs substance and finished products. To date, the effect of light on JJ is not studied, in this study photostability evaluation of JJ was carried out. The test sample was manufactured with genuine ingredients in the in-door pharmacy of the National Institute of Unani Medicine. JJ was packed in two transparent polyethylene terephthalate airtight containers. The first sample was analysed at zero-day and the second sample was placed in a stability chamber subjected to light challenge with an overall illumination of 1.2 million lux hours combined with near ultraviolet energy of 200-watt hours per square meter by using option 2, along with 30±2°C temperature and relative humidity 70±5%. Analysis of both finished products showed no considerable changes in organoleptic characters. Less than 5% variation was observed in physicochemical parameters. HPTLC fingerprinting showed justifiable variation. Microbial load and specific counts were within the limit prescribed by WHO. As no unacceptable changes were noted in JJ subjecting to light challenge, it is concluded that JJ is a photostable Unani compound formulation.

Haleema Aneesa K(Department of Niswan wa Qabala, Markaz Unani Medical College) ; Mariyam Roqaiya(Department of Niswan wa Qabala, Luqman Unani, Medical College, Hospital and Research Centre) ; Mohd Aqil Quadri(Department of Niswan wa Qabala, Luqman Unani, Medical College, Hospital and Research Centre) pp.19-19 https://doi.org/10.5667/CellMed.2021.0019
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Abstract

Background: Dysmenorrhea is the most common menstrual complaint in young women with a prevalence as high as 90% and is responsible for substantial repeated short-term absenteeism from school and work in young women. The objective of this study was to compare the efficacy of Commiphora myrrha and honey with mefenamic acid in primary dysmenorrhea. Materials and Methods: This prospective standard controlled trial was conducted at Luqman Unani Medical College Hospital and Research Center Vijayapura, India where 40 diagnosed patients of primary dysmenorrhea were randomly assigned to receive test drug (powdered Commiphora myrrha gum resin10g with 30g honey in two divided doses) or active control drug (mefenamic acid 250mg TID) for first 3days of menstruationfor two consecutive cycles. The primary outcome measure was reduction in severity of pain assessed by numerical pain rating scale (NPRS), and secondary outcome measures were improvement in quality of life (QOL) assessed by SF-36 and reduction in perceived stress score (PSS). Results: During first cycle treatment no significant difference was found in NPRS score (p=0.085) between the groups however significant difference in NPRS score (p<0.001) was seen during 2nd treatment cycle. Significant reduction (p=0.022) in the perceived stress score was noted and overall quality of life was markedly improved after treatment in both the groups. Conclusion: These data suggest that Commiphora myrrha gum resin with honey is an effective herb in reducing symptoms of primary dysmenorrhea. These results need to be confirmed by a properly designed trial with a larger sample size. Trial registration: Clinical Trial Registry India CTRI/2017/09/009596.

Arshiya Sultana(Dept. of Amraze Niswan wa IlmulQabalat (Gynecology and Obstetrics), National Institute of Unani Medicine) ; Marhaba Khanam(Dept. of Amraze Niswan wa IlmulQabalat (Gynecology and Obstetrics), National Institute of Unani Medicine) ; Khaleequr Rahman(Dept. of Ilmul Saidla (Pharmacy), National Institute of Unani Medicine) ; Sumbul(Dept. of Amraze Niswan wa IlmulQabalat (Gynecology and Obstetrics), National Institute of Unani Medicine) pp.20-20 https://doi.org/10.5667/CellMed.2021.0020
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Abstract

Background: The pandemic COVID-19 caused by a novel coronavirus SARS-COV-2 has spread like a forest fire. This disease may have serious consequences for pregnant women. Presently, no specific drugs or vaccines exist to battle this disease and researches are underway. Unani medicine has a unique role in prevention and management during epidemics. Here, we reviewed the overview of COVID-19 infection and pregnancy, concept and practices in Unani medicine for flu-like epidemics in general and pregnancy, and safety of Unani drugs for the prevention and treatment of mild symptomatic cases of COVID-19 during pregnancy. Methodology: Unani classical texts and pharmacopoeia were meticulously explored for concepts and practices for flu-like epidemic diseases. Further, we browsed scientific databases such as PubMed, Scopus and others for an overview, epidemics and Unani medicine, effectiveness and safety of Unani drugs in COVID-19 and pregnancy. Results: Unani medicine includes prevention and management of flu-like epidemic include quarantine and isolation, aromatic herbal drugs fumigation and spraying for environmental disinfection, ilaj bid tadbir for health promotion and use of health-protecting drugs and symptom-specific drugs in general and related to pregnancy. Lahsun, asalussus, behidana, banafsha, zanjabeel, unnab, etc are in use since antiquity for the prevention and treatment of asymptomatic and mildly symptomatic pregnant women during infectious and epidemic diseases. Conclusion: Currently, the aforementioned plants are proven for antiviral, antioxidant, immunomodulatory and anti-inflammatory activities, probably useful in the COVID-19 pandemic. Additionally, scientific studies have provided new insight into the mechanism underlying the therapeutic effect of Unani medicines that are safe in pregnancy.

Arjumand Naaz(P.G Department of Ilmul Advia (Pharmacology), National Research Institute of Unani Medicine for Skin Disorders) ; Uzma Viquar(P.G Department of Ilmul Advia (Pharmacology), National Research Institute of Unani Medicine for Skin Disorders) ; Mohammad Abdul Rasheed Naikodi(Drug Standardization Research Unit, National Research Institute of Unani Medicine for Skin Disorders) ; Javed Inam Siddiqui(P.G Department of Ilmul Advia (Pharmacology), National Research Institute of Unani Medicine for Skin Disorders) ; Mohammad Zakir(Department of Ilmul Advia (Pharmacology), National Research Institute of Unani Medicine for Skin Disorders) ; Munawwar Husain Kazmi(Department of Ilmul Advia (Pharmacology), National Research Institute of Unani Medicine for Skin Disorders) ; Ahmed Minhajuddin(National Research Institute of Unani Medicine for Skin Disorders) pp.21-21 https://doi.org/10.5667/CellMed.2021.0021
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Abstract

Background: Unani System of Medicine (USM) has its origin to Greece. To ensure and develop the quality, authenticity of Unani drugs, standardization on modern analytical parameter is essential requirement for drugs. Objectives: The aimed of the present study was to develop a standard profile of "Qurṣ-e-Mafasil" by systematic study through authenticated ingredients, pharmacognostic identification followed by physicochemical, TLC, HPTLC fingerprinting analysis as per standard protocol. Material and Methods: In this study three batches of "Qurṣ-e-Mafasil" QM were prepared by standard method as per UPI had been followed by organoleptic properties of formulation such as appearance, color, odor, taste. Powder Microscopy and physicochemical studies were carried out such as Uniformity of weight, Friability, Disintegration time, hardness, LOD, ash vales and extractive values in like aqueous, alcohol & hexane. Further qualitative tests such as Thin-Layer Chromatography (TLC), and High-Performance Thin Layer Chromatography (HPTLC) studies were also carried out to develop fingerprint pattern of the alcoholic solvent extract of QM. Phytochemical screening was carried out in different solvent extracts such as alcoholic, aqueous and chloroform extracts to detect the presence phytoconstituents in the formulation QM. Heavy metals, Microbial Load Contamination and pesticidal residues were also determined. Results: Qurṣ-e-Mafasil showed tablet-like appearance, light brown colour, mild pungent odour and acrid taste. Uniformity of weight (mg), friability (rpm), and hardness (kg/cm) and disintegration time was ranged between (500 to 503), (0.0340 to 0.038), (8.40 to 8.67) and (4-5 minutes) respectively for the three batches. Loss in weight on drying at 105˚C was ranged between (8.3425 to 8.7346). Extracted values were calculated in distilled water ranged between (30.9091 to 31.4358), hexane (1.1419 to 1.4281), and alcohol (3.3352 to 3.3962). The ash values recorded were ranged between (3.7336 to 3.8378), and acid insoluble ash (0.5859 to 0.6112).

CELLMED