Aim:The present research work was undertaken to describe various clinical signs and hematobiochemical alterations in dogs affected with Babesia gibsoni.Materials and Methods:Blood smears from a total of 79 suspected dogs of Anand region as well as Surat region of Gujarat state (India) were screened for detection of intraerythrocytic piroplasm of small form of Babesia. Diagnosis was made on the basis of clinical signs and demonstration of B. gibsoni organism in Giemsa-stained thin blood smears. The clinical signs were recorded at the time of presentation, and blood samples were subjected to estimation of hematobiochemical parameters by auto hematology analyzers at College of Veterinary Science and Animal Husbandry, Anand. Statistical analysis, interpretation, and comparison of hematobiochemical changes with scientific literature were carried out to understand the pathophysiology of the disease.Results:Out of 79 dogs, 16 were positive for naturally occurring babesiosis based on the presence of intraerythrocytic piroplasm of small form of Babesia in blood smears. The clinical cases were manifested by wide variety of non-specific clinical signs. The hematological evaluation revealed that the mean values of hemoglobin and total erythrocyte counts in dogs with babesiosis decreased significantly (p<0.01) in comparison to healthy dogs. Among differential leukocyte count, mean values of neutrophils and eosinophils increased while lymphocytes decreased (p<0.01) in dogs with babesiosis in comparison to healthy dogs. Serum biochemistry revealed increase (p<0.01) value of alkaline phosphatase, alanine aminotransferase, aspartate aminotransferase, and globulin as well as decrease in albumin levels (p<0.05) in dogs with babesiosis as compared to healthy dogs.Conclusion:B. gibsoni is having multisystemic effects with atypical hematobiochemical changes in dog are discussed here, which would aid new insights in diagnosis of disease.

Aim:This study was planned to reveal the clinical signs and biochemical alterations in pregnancy toxemic goats.Materials and Methods:Blood samples were collected from 20 healthy pregnant and 45 pregnancy toxemic goats and analyzed biochemically.Results:The most significant clinical findings were observed in naturally affected goats with pregnancy toxemia included anorexia, recumbency, lethargy, opisthotonos, dropped head, periodic convulsion, sweetish fruity odor from breath, apparent blindness, bloat, grinding of teeth, and frothy salivation. In this study, the level of serum glutamic-oxaloacetic transaminase (SGOT) (84.23±1.44 IU/L), serum glutamic pyruvic transaminase (SGPT) (216.01±4.07 IU/L), blood urea nitrogen (BUN) (22.24±0.31 mg/dl), creatinine (2.13±0.09 mg/dl), β-hydroxybutyric acid (BHBA) (0.46±0.83 mmol/L), and non-esterified fatty acid (NEFA) (1.67±0.71 mmol/L) was significantly higher whereas glucose (30.89±0.38 mg/dl) and calcium (8.10±0.20 mg/dl) levels were significantly decreased in pregnancy toxemic goats as compared to healthy goats.Conclusion:The goats with pregnancy toxemia exhibited clinical signs include anorexia, recumbency, sweetish fruity odor from breath, apparent blindness, bloat, grinding of teeth, and frothy salivation. Biochemically, there were significantly decreased the level of glucose and calcium, and increased level of SGPT, SGOT, BUN, creatinine, BHBA, and NEFA in the pregnancy toxemic goats.

The present research work was undertaken to assess the etiopathology and haematobiochemical alterations in anemic dogs of Anand region, Gujarat irrespective of their age, sex and breed. Total 78 dogs were screened for anemia and blood samples were collected from a 51 anemic dogs of Anand region of Gujarat to identify etiopathology and haematobiochemical parameters alterations. Statistical analysis, interpretation, different etiology and comparison of haematobiochemical alteration with scientific literature were carried out to understand pathophysiology of disease. Amongst 78 of 51 dogs, incidence of anemia was recoded 65.38 per cent in which highest was due to liver disorders (23.53%). Incidence of anemia was observed higher in in adult group (58.83%) as well as in male (52.94%). Most clinical variants of anemic dogs showed pale mucous membrane (86.27%), hypothermia (68.63%), tachycardia (70.59%), tachypnea (74.51%) and increased capillary refilling time (64.71%). Haematological indices of anemic dogs revealed Hb, TEC, PCV, MCH, MCHC and MCV decreased significantly (p<0.01), whereas TLC increased significantly (p<0.05) as compare to healthy dogs. Serum biochemistry revealed significantly (p<0.01) increased BUN, Creatinine, Glucose, AST and ALT levels as well as decreased in total protein level in anemic case as compare to healthy ones. Different etiological factors for developing in anemia in dogs as well as hematobiochemical alterations are mentioned, which will be useful for further detailed investigations and therapeutic management.

A simple and sensitive spectrophotometric method has been developed for simultaneous determination of Meropenem and Sulbactam in a binary mixture. In the proposed method, the absorbances were measured at 296.0 nm and 258.0 nm corresponding to the absorbance maxima of Meropenem and Sulbactam in 0.1 N Sodium Hydroxide respectively. Linearity range was observed in the concentration range of 5-25 μg/ml for Meropenem and 2.5-12.5μg/ml for Sulbactam. Concentration of each drug was obtained by using the absorptivity values calculated for both drugs at two wavelengths, 296.0 nm and 258.0 nm and solving the simultaneous equation. Developed method was applied to laboratory mixture. The method was validated statistically and recovery study was performed to confirm the accuracy of the method. The method was found to be rapid, simple, accurate and precise.

Background: We developed a selective bioanalytical RP-HPLC method for estimation of vitamin E from dried blood spot (DBS) sample, a potential technique which can be used for population-based epidemiological studies. Vitamin E was extracted from DBS by using liquid-liquid extraction technique with methanol (100% v/v) as reconstituting solvent for the residue. Alpha tocopheryl acetate was used as internal standard. Samples were analyzed directly on HPLC with C 18 (250 × 4.6 mm × 5 μm) Phenomenex column. The mobile phase used was methanol to water (99:1% v/v) at a flow rate of 1.4 mL/min. The detector wavelength used was 292 nm. Results: The retention time observed for vitamin E and internal standard was 10.225 ± 0.00075 min and 13.580 ± 0.00075 min respectively. The vitamin E calibration curve was found to be linear over the range of 0.625 to 60 μg/ mL. The limit of quantification for vitamin E was found to be 0.1 μg/mL. Accuracy of the developed method was found to be 103.179%, 101.625%, and 100.174% with percentage of coefficient of variation of 0.0161, 0.0215, and 0.2790 for HQC, MQC, and LQC samples respectively which were within USFDA acceptance limit of ± 15 to ± 20%.The intraday and interday precision expressed as coefficient of variation were 0.0191-0.0841% and 0.0074-0.0252% respectively. Conclusions: The method represents a simple, rapid, specific, accurate, and precise method for estimation of vitamin E in human blood using DBS technique. The developed method can be further evaluated with respect to effect of matrix variability before it can be used in clinical setting.