Theses

Browse

Search Results

Now showing 1 - 9 of 30

Open Access
Evaluation of hepatoprotective effect of ethanolic extract of eugenia jambolana (njaval) leaves on paracetamol induced toxicity in rats
(Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences Mannuthy, 2008) Midhun, M V; Aravindakshan, C M
Open Access
Hypolipidaemic effect of allium sativum and emblica officinals in rabbits
(Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, 1992) Mini, K P; KAU; Gopakumar, N
The study was undertaken with the objective of determining the hypolipidaemic effect of Allium sativum and Emblica officinalis in hyper lipidaemic rabbits. The different forms of the indigenous agents tried were aqueous extract of A. sativum and fruit pulp as well as aqueous extract of E. officinalis. The effects produced by the above agents were compared with that of the known hypolipidaemic drug namely, Gemfibrozil which served as the positive control drug. Thirty Newzealand white adult male rabbits were used for the study. The average body weight of the animals were 1.5 kg. They were housed in cages designed for the purpose. Each rabbit received 200 g standard rabbit’s feed per day. The experiment was conducted in two stages. The first step was to render all the rabbits hyper chloesterolaemic. In order to achieve this goal, the standard ration was supplemented daily with 100 mg cholesterol and 8 g Vanaspathi for each rabbit. The rabbits were fed on this diet continuously for 60 days when they developed hypercholesterolaemia. This was ascertained by the estimation carried out initially and every fortnightly during this period. The parameters estimated were plasma cholesterol and plasma triglyceride. The second part of the study was to evaluate the hypolipidaemic efficacy of the chosen indigenous preparations in comparison to that of Gemfibrozil. Each agent was tried on a separate group by dividing the hypercholesterolaemic rabbits into five groups of six each. Group I was kept as the control group which received no treatment. Group II was administered aqueous extract of A. sativum 10 ml (2g/kg b.wt.) orally. The animals of Group III were treated with fruit pulp of E. officinalis at a dose rate of lg/kg orally. Group IV animals received aqueous extract of E. officinalis, orally at a dose rate of I g/kg prepared in 10 ml of water. The Group V served as the positive control which received Gemfibrozil at a dose rate of 120 mg/kg orally. All the drugs were administered for a period of 75 days. The high cholesterol containing diet was continued throughout the period of study. The difference brought about by the above agents on plasma cholesterol and triglyceride of hyperlipidaemic rabbits was determined by routine estimations of the above parameters carried out every fortnightly. At the end of the period of study histopathological studies of liver and aorta were also performed in order to detect the structural changes in tissues caused by the different treatments. The control group of animals increased their plasma cholesterol and triglycerids by 76.59 and 81.36% respectively. This increase was found to be statistically significant. The liver and aorta of these animals also supported the above finding on histopathological examination. Diffused fatty changes was noticed throughout the section of liver and aorta. The hepatocytes were filled with fat and the nucleus was displaced. Lining of the wall of aorta also showed severe fatty infiltration in the control group. It was found that administration of aqueous extract of A. sativum reduced plasma cholesterol by 79.08 per cent and plasma triglycerides by 75.76 per cent within a period of 75 days. Both the reductions were highly significant. Compared to the control group, the histopathological findings of this group showed that garlic was very effective in counteracting the fatty changes induced by high cholesterol diet in rabbits. The fatty changes of liver was only of a mild degree and the fatty infiltration of aorta was also very mild. The percentage reduction obtained in the case of fruit pulp of E. officinalis was 69.74 and 78.20 with respect to cholesterol and triglycerides which was also statistically significant. Aqueous extract of E. officinalis administered to the fourth group of animals could produce a reduction in plasma cholesterol and triglyceride by 79.40 per cent and 82.80 per cent respectively. The histopathological studies conducted in the above two groups showed almost similar findings. Compared to the control group, the degree of fatty changes was only mild to moderate. Infiltration of fat into the elastic tissues of aorta was also very mild. Hence it can be suggested that E. officinalis is capable of counteracting the fatty changes in liver and aorta partially. Gemfibrozil which served as the positive control brought about a percentage reduction of 78.43 with respect to cholesterol and 81.54 per cent in the case of triglyceride, both were found to be highly significant. The above observation was well supported by the photomicrographs of liver and aorta taken from the animals of this group. Mild to moderate degree of fatty changes was noticed in the liver and aorta. Aorta did not reveal prominent changes like that of the control group due to fatty infiltration. The histopathological observation made in the case of Gemfibrozil resemble that of E. officinalis. From the results of the present study, it can be inferred that aqueous extract of A. sativum and fruit pulp as well as aqueous extract of E. officinalis are effective as hypolipidaemic agents and this finding is further asserted by the simultaneous histopathological studies carried out. Both the indigenous agents were capable of correcting the fatty changes produced by the fat containing diet to a considerable extent and garlic was found to be superior to E. officinalis in this respect. The efficacy of these agents in lowering plasma cholesterol and triglyceride was comparable to that of Gemfibrozil as shown by the statistical analysis of the results obtained. Hence these agents prove to be of value as hypolipidaemic agents in the future clinical trials that can be carried out in animals and also in human beings.
Open Access
Assessment of the antipyretic and analgesic effect of selected indigenous plants in rats
(Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, 1992) Suresh, B; KAU; Marrykutty, P
The experiments were conducted in three different parts. In the first part of the experiment the antipyretic activity of Ocimum sanctum and Tinospora cordifolia was determined. Twenty four groups of ten albino rats each were used for the study. Pyrexia was induced by injecting 20 per cent yeast suspension subcutaneously. Benzene extract of O. sanctum was given at 50, 100, 200 and 400 mg/kg dose levels in four different groups. A dose dependent reduction in temperature was obtained after four hours of its administration. Four hundred mg/kg dose level produced an affective lowering in the temperature than other doses used and showed the reduction in the temperature from 38. 840 C to 37. 590 C . Dose rates used for essential oil of O. sanctum were same as benzene extract. Two hundred mg/kg dose level revealed a more effective reduction in the temperature than four hundred mg/kg. A reduction of temperature was observed from 39. 370 C to 37. 960 C after four hours of its administration. Single, double and triple the doses of decoction of O. sanctum were used for antipyretic study. Compared to other doses, double the dose of decoction produced a maximum reduction in the temperature. It produced a reduction from 38. 930C to 37.490 C. Dose rate used for benzene extract of T. cordifolia were 50, 100, 200 and 400 mg/kg body weight. A dose depandant reduction in the temperature could be observed after four hours of its administration. Four hundred mg/kg dose level revealed as an effective dose caused a reduction from 39.010 C to 37.770 C after four hours of its administration. Single, double and triple the dose of decoction of T. cordifolia were used for assessing antipyretic activity. Double the dose of decoction was found to be more effective. And it reduced the temperature from 39.720 C to 38.140 C after four hours of its administration. In the second part of the experiment analgesic effect of benzene extract of O. sanctum and T. cordifolia were evaluated. All the dose rates of both the drugs used were compared with aspirin for a period of two hours showed no significant analgesic effect. In the third part of the experiment long term effect of essential oil of O. sanctum and benzene extract of T. cordifolia were studied. Haematological parameters were determined at an interval of 15 days. Benzene extract of O. sanctum and T. Cordifolia produced a significant charge in the erythrocyte count from 45 days onwords. At the end of the study Benzene extract of T. cordifolia treated group revealed a significant change in the leucocyte count. Both the groups showed a significant change in the haemoglobin value from days onwards. Fifteen days after the administration of the drug, both the groups showed a significant increase in the neutrophil count and decrease in the lymphocyte count. At the end of study same effect was noticed. On 61st day histopathological studies of liver were conducted. Lesions observed in both the treated groups were in general, comparable with those of control group. It was found that neither essential oil of O. sanctum nor benzene extract of T. cordifolia caused lesions in hepatic tissue in any of the experimental animals.
Open Access
Influence of buprenorphine , pentazocine and xylazine analgesia on ketamine anaesthesia in dogs
(Department of Pharmacology, College of Veterinary and Animal Sciences, Mannuthy, 1989) Usha, P T A; KAU; Rajagopalan, N K
The experiments were conducted in three different parts. In the first part of the experiment the ED50 of the three drugs namely buprenorphine, pentazocine and xylazine was determined using the analgesiometer (tail flick method) in rats and tail clip method in mice. The ED50 of buprenorphine in rats and mice was 0.25 + 0.084 mg/kg and 0.9827 + 0.0751 mg/kg intraperitoneally. The ED50 of pentazocine in rats was 32.60 + 0.071 mg/kg and in mice 48.50 + 0.323 mg/kg. The ED50 of xylazine for analgesia in rats and mice was 1.424 +0.229 mg/kg and 7.523 + 0.47 mg/kg respectively. In the second part of the experiment the influence of buprenorphine, pentazocine and xylazine analgesia on ketamine anaesthesia in dogs were studied. Twenty – four animals divided into four groups (A(K), B(X-K), C(B-K) and D(P-K) were administered with ketamine (20 mg/kg), xylazine (2 mg/kg) plus ketamine (15 mg/kg), buprencrphine (0.03 mg/kg) plus ketamine (15 mg/kg) and pentazocine (2 mg/kg) plus ketamine (15 mg/kg) respectively. The sternal recumbency time, clinical signs, duration of anaesthesia, regaining of sternal recumbency time, mean standing time, total recovery time and haemogram were studied. The sternal recumbency time was minimum in xylazine administered group. Untoward reactions like salivation and rigidity of the muscles were observed in groups A(K) and D(P-K). There was significant reduction in rectal temperature in all the groups. The pulse rate was elevated in group A(K) and depressed in group B(X-K), while a transient increase followed by decrease showed in group C(B-K) and D(P-K) . Respiratory depression was observed in groups C(B-K) and D(P-K). Average duration of anaesthesia was maximum in group B(X-K) while all other groups showed almost similar durations of anaesthesia. The time for regaining of sternal recumbency was also maximum in group B(X-K), then the groups A(K), C(B-K) and D(P-K) respectively. Mean standing time was maximum in group B(X-K). The rest of the groups followed the same pattern as above. The total recovery time was maximum in group C(B-K), then group B(X-K), A(K) and D(P-K) respectively. The study of haemogram showed that, the haemoglobin, packed cell volume and erythrocyte counts decreased at 30 min. after drug administration in groups A(K) and B(X-K) while there was no significant variation in group C(B-K) and D(P-K). The group D(P-K) showed a significant reduction in leucocyte count, while there were no variations in other groups observed. In the third part of the experiment the reversal of anaesthesia using the 2 blocker yohimbine was studied. Twenty-four animals divided into four groups (E,F, G and H) were administered with the same drugs as in the second part of the experiment. Along with that yohimbine (0.25 mg/kg in group E, G and H and 2 mg/kg in group F) was administered 15 min. later. The groups E, F, G and H were designated as K-Y, X-K-Y, B-K-Y and P-K-Y respectively. Uptoward effects exhibited after yohimbine administration were salivation, panting and hyperaesthesia during recovery. Rectal temperature, pulse and respiration were increased in all the groups. The duration of anaesthesia, regaining of sternal recumbency time, mean standing time and total recovery time were significantly reduced in group F(X-K-Y), while there was no variation in the above parameters in group E(K-Y). Only the total recovery time significantly reduced in group G(B-K-Y) and prolongation of standing time and total recovery time was observed in group H(P-K-Y). The haematological changes noticed in the second part of the experiment were completely reversed by yohimbine.
Open Access
Identification of toxic fractions of Mimosa invisa (Anathottavadi) and its toxicity in rabbits
(Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, 2007) Usha, P T A; KAU; Gopakumar, N
The present study was undertaken to identify the toxic fraction of Mimosa invisa in rabbits and to assess to toxicity of Mimosa invisa fresh juice, cold alcoholic extract and various fractions of alcoholic extract utilizing rabbit as a model along with treatment study. The experiment was conducted in two phases. The first part of the study involved assessment of toxicity of fresh juice of Mimosa invisa (group II) and cold alcoholic extract (group Ill). Group I served as control. The preliminary tests were conducted to derive the toxic dose of fresh juice and alcoholic extract of Mimosa invisa. The toxic doses were 25 g/kg and 1 g/kg body weight for Mimosa invisa fresh juice and alcoholic extract respectively. The clinical symptoms, biochemical parameters and haemogram were observed to assess the toxicity. The serum ALT, AST and GGT levels showed significant increase in both the groups. The serum creatine kinase levels exhibited an increase followed by a decrease. There was a significant increase in serum creatinine and urea levels. There were no changes in serum total protein, albumin, globulin and albumin-globulin ratio. Significant decrease in VPRC, haemoglobin and RBC count could be noticed. The erythrocyte indices did not show any variations. The leucocytosis was observed in group II and III when compared to control (group I). Lymphocytosis with neutropenia were also observed in both the groups. The second phase of the study involved identification of toxic dose of each fraction of Mimosa invisa: The preliminary studies revealed that chloroform fraction (Fraction I) and water insoluble residue (fraction IV) were not toxic to rabbits while the fraction II (n-butanol fraction) and fraction III (aqueous fraction) were toxic to rabbits. Hence the two toxic fractions were pooled and used for further studies. It was found that 0.4 g/kg of pooled toxic fraction was toxic in rabbits. The toxicity was assessed by the evaluation of clinical symptoms, biochemical parameters and haemogram. The group V (pooled toxic fraction) showed inappetence, dullness, lethargy and reluctant to move. A significant increase in serum ALT, AST and GGT levels were observed. The serum ALP levels showed an increase followed by a decrease. The serum creatine kinase also showed similar increase followed by decrease. The creatinine and urea levels exhibited a continuous increase in group V. There were no changes in total protein, albumin, globulin and albumin-globulin ratio. The VPRC, RBC and haemoglobin showed significant decrease but there were no changes in erythrocyte indices. A significant leucocytosis was observed in group V. The differential leucocyte count showed lymphocytosis with neutropenia. The group VI (Half the toxic dose of pooled toxic fraction) failed to produce toxicity as evidenced by biochemical parameters and haemogram. The group VII (Double the toxic dose of pooled toxic fraction), all the animals died within 12-24 hours of administration of the dose. The group VIII animals were treated with a decoction prepared from equal quantities of Boerhvia diffusa, Hygrophila auriculata and Tribulus terrestris along with pooled toxic fraction of Mimosa invisa. The prominent symptom of inappetence was only for a short period of time (1-2 day). Then the animals started taking normal feed and water. The serum AL T, AST and GGT levels were significantly increased during the first five days, then the values returned to normal level. The serum creatine kinase and ALP levels did not show significant changes. The serum creatinine and urea levels showed significant increase followed by decrease. All the parameters showed significant improvement when compared with group V (pooled toxic fraction alone). There were no changes in serum protein, 'albumin, globulin and albumin-globulin ratio. The screening of alcoholic extract and various fractions revealed that the alcoholic extract n-butanol fraction and aqueous fraction contained steroids phenolic compounds, tannins, flavonoids, glycosides, diterpenes triterpenes and saponins. The chloroform fraction was positive for flavonoids only, whereas water insoluble fraction contained flavonoids and traces of tannins, triterpenes and saponins. From the results of the present study, it is concluded that the phytotoxin present in M invisa is nephrotoxic and hepatotoxic. The treatment schedule tried using a decoction of Boerhavia diffusa, Tribulus terrestris and Hygrophila auriculata could protect kidney and liver from the phytotoxin present in M invisa. Further study is needed to isolate the phytotoxin present in M invisa so that a specific antidote can be developed.
Open Access
Assessment of the antifertility property of ocimum sanctum
(Department of Pharmacology and Toxicology, College of Veterinary and Animal Sciences, Mannuthy, 1979) Girisdan, K; KAU; Jacob Cheeran, V
A study was carried out in rats, to assess the antifertility property of the benzene fraction of the leaves of the plant Ocimum sanctum. Premating treatment was done in female animals at does levels of 200 and 400 mg per kilogram body weight for a duration of eight days. Male animals were subjected to the treatment at a dose level of 200 mg per kilogram body weight for 20 days . The experimental animals were allowed to mate with untreated animals of the opposite sex. Histopathological examination of the organs – pituitary, ovary, tests, liver and kidney were carried out. Results of the study suggested considerable reduction of fertility in both the sexes. This can be attributed to the impaired release of gonadotrophic hormones and the resulting improper functioning of the gonads. Administration of the extract showed no toxic effects in the treated rats as well as in their offspring.
Open Access
Assesment of cadmium toxicity in cattle of Eloor industrial area
(Department of Veterinary Pharmacology and Toxicology,College of Veterinary and Animal Sciences, Mannuthy, 2001) Nisha, A R; KAU; Chandrasekharan, A M Nair
A study was undertaken to assess impact of environmental pollution with cadmium in cattle of Eloor industrial belt. Areas around Fertilizers and Chemicals Travancore (FACT), India, Aluminium Company (INDAL), Binani Zinc and Hindustan Insecticides Limited (HIL) were selected for the study. As the first step, retrospective analysis of case sheets was done in Eloor and Muppathadam Veterinary hospitals. In Eloor veterinary hospital out of the 1503 case sheets examined 851 digestive disorders, 126 repeat breeders, 75 respiratory diseases and 41 deficiency diseases were observed. Out of 5920 case sheets analysed in Muppathadam veterinary hospital 3348 digestive disorders, 1284 repeat breeders 398 respiratory diseases and 433 deficiency diseases were observed. Disease conditions like digestive disorders, deficiency diseases and repeat breeders are suggestive of cadmium toxicity. The field samples like water and forages, biological samples like blood, serum, urine dung and milk were collected from cattle in the industrial field localities. The cadmium content in this field and biological sample were estimated by Atomic Absorption Spectrophotometer. Animals kept in the University Livestock Farm, Mannuthy were taken as controls. Field samples like water and fodder were also collected from area around University Livestock Farm, Mannuthy. The cadmium content of water from Alupuram, Binanipuram, Eloor south, Eloor north ranges from 0.03 – 0.04 ppm. These were significantly higher than controls (0.01 ppm). The cadmium content of fodder from Alupuram, Binanipuram, Eloor south, Eloor north ranges from 2.60 – 6.53. These were also significantly higher than controls (0.65 ppm). The cadmium level of blood, serum, milk, urine and dung from cattle of Alupuram, Binanipuram, Eloor south and Eloor north were significantly higher than controls. Haematologocal values like total erythrocyte count, haemoglobin and packed cell volume showed significant decrease in catle of test areas than controls. Other haematologic values like differential leucocyte count, total leucocyte count, mean corpuscular volume, mean corpuscular haemoglobin and mean corpuscular haemoglobin concentration did not show any significant changes. Total serum protein and albumin values from cattle of Alupuram, Binanipuram, Eloor south and Eloor north were significantly lower than control values. Serum enzymes like aspartate amino transferase, alamine amino transferase and alkaline phosphatase levels were higher in cattle from test areas than controls. It can be concluded that field and biological samples collected from the vicinities around Fertilizers and Chemicals, Travancore (FACT), Binani Zinc and Indian Aluminium Company (INDAL) are contaminated with cadmium.
Open Access
Studies on the Effect of Corticosteroids, Neostigmine and Calcium in Cobra Venom (Naja naja) Intoxication
(Department of Veterinary Pharmacology and Toxicology,College of Veterinary and Animal Sciences, Mannuthy, 1975) Venugopalan, K; KAU; Nair, K P D
Administration of specific antiserum as early as possible after snake bite is of utmost importance for better chances of survival. Supportive measures are definitely capable of reducing the venom toxicity And prolonging survival period eg., if the absorption of venom from the site of bite could be delayed or retarded it will be highly beneficial to the patient. It has been shown that certain drugs are capable of decreasing capillary permeability and altering the rate of absorption of venom from the site while other agents may alleviate neurotoxicity or reduce haemotoxicity of venoms on the system. The present study was undertaken to evaluate the beneficial effect of (1) ‘Betnesol’ (Glaxo brand of betamethasone), (2) Neostigmine bromide (E Merck) and (3) Calcium gluconate – 10% (Sandoz) in experimental envenomation with cobra venom (Naja naja) in adult rats of both sexes. One LD50 cobra venom (0.097 mg per 100 g body weight – death within 8 hours) was given intramuscularly to these experimental rats and the trial drugs viz., ‘Betnesol’ (0.6, 0.8 and 1 mg per 100 g body weight), neostigmine bromide (30 mcg per 100 g body weight) and calcium gluconate (8,10 and 12 mg per 100 g body weight) were given intraperitoneally at varying intervals to evaluate the efficacy to these drugs in respect of their ability to prolong the survival period of experimentally envenomated rats. It is observed that ‘Betnesol’ at dose rate of 0.8 to 1 mg per 100 g body weight of rate when given immediately after injection of one LD50 cobra venom gave 100 percent prolongation of survival period and the degree of protection decreases when the time lag for the administration of this drug. Neostigmine bromide was found to be of not much value to counteract the neurotoxicity produced by cobra venom. Results of calcium administration were of a varying nature and require further investigation.
Open Access
Antibacterial and antifungal activity of selected medicinl plants available in Kerala
(Department of Veterinary Pharmacology and Toxicology,College of Veterinary and Animal Sciences, Mannuthy, 2010) Sabitha, Jose; KAU; Usha, P T A
In the present study cold ethanolic extract and fresh juice of five medicinal plants were screened for their in vitro antibacterial and antifungal activities. The plants were Annona squamosa (Aatha), Cassia alata (Anathakara), Coleus amboinicus (Panicoorka), Myristica fragrans (Nutmeg) and Tectona grandis (Teak). Antimicrobial activity was tested against Staphylococcus aureus subsp.aureus (MTCC 96), Salmonella enteritidis (MTCC 3219), Escherichia coli (MTCC 723), Pasteurella multocida subsp.multocida (MTCC 1161), Pseudomonas aeruginosa (MTCC 741), Aspergillus fumigatus (MTCC 870), Candida albicans (MTCC 227) and Cryptococcus neoformans var neoformans (MTCC 4404). Phytochemical analysis was conducted for the presence of routine secondary plant metabolites. The diameter of inhibitory zone at various concentrations of the extract, minimum inhibitory concentration (MIC), minimum bactericidal concentration (MBC) and minimum fungicidal concentration (MFC) were used to evaluate the in vitro antimicrobial activity of the above mentioned plants. Disc diffusion method, microtitre plate dilution technique and broth dilution technique were used. The reference drugs used in this study were penicillin G, furazolidone, ketoconazole and clotrimazole. The maximum yield was obtained from ethanolic extract of A. squamosa leaves (18.07 per cent). Leaves of C. amboinicus produced the maximum amount of fresh juice among the five plants (8 ml from 10 g of the fresh tender leaves). Phytochemical analysis reported the presence of steroids, alkaloids, tannins, flavonoids, glycosides, phenolic compounds, diterpenes, triterpenes and saponins in the leaves of A. squamosa and C. alata. Alkaloids, tannins, flavonoids, glycosides, steroids and saponins were present in the leaves of C. amboinicus. M. fragrans leaves contain glycosides, flavonoids, saponins and phenolic compounds. Qualitative chemical tests revealed the presence of tannins, flavonoids, glycosides, phenolic compounds and saponins in the leaves of T. grandis. All the extracts showed varying degrees of antimicrobial activity on the microorganisms tested. The antimicrobial screening revealed the susceptibility of E. coli to A. squamosa, C. amboinicus and T. grandis. The growth of S. aureus, P. multocida and P. aeruginosa was inhibited by all the five plants. S. enteritidis was found to be susceptible to T. grandis, M. fragrans and C. amboinicus. MIC values ranged from 200-1000 µg/ml and MBC values ranged from 500-1000 µg/ml. In case of A. squamosa, MBC value against E. coli was more than 1000 µg/ml. The antifungal screening revealed that the growth of C. albicans was inhibited by C. alata, C. amboinicus, M. fragrans and T. grandis. A. squamosa and C. alata inhibited the growth of C. neoformans. A. fumigatus appeared to be susceptible to A. squamosa, C. alata and C. amboinicus. MIC values ranged from 250-1000 µg/ml for the fungal strains. MFC values ranged between 500-1000 µg/ml except for A. squamosa and C. alata. MFC of C. alata against A. fumigatus and C. albicans was more than 1000 µg/ml. MFC of A. squamosa against C. neoformans was found to be more than 1000 µg/ml. The growth of S. aureus was inhibited by fresh juice of A. squamosa, C. amboinicus, M. fragrans and T. grandis leaves. E. coli was susceptible to fresh juice of C. amboinicus leaves. Fresh juice of C. alata was found to be effective against C. albicans. P. aeruginosa was inhibited by fresh juice of M. fragrans leaves. All the plants under the study were found to possess antimicrobial properties, thereby justifying their popular use in the treatment of infectious diseases caused by resistant microorganisms. Further study is required to assess the in vivo efficacy of these plants for the said action.

Theses

Browse

Thesis Type

Type

Author

Date

Subject

Advanced Search

Settings

Sort By

Results per page

Search Results