“
“GOD was covalently immobilized U0126 on polymer/silica gel hybrid support prepared by coating high surface area of silica gel with modified acrylonitrile co-polymer. The relationship between immobilization factors and enzyme activity were examined by the series of contour plots. The selections of the immobilization variable range were extremely

precise in the 3-level-3-factor fractional design. The results indicated that the optimal conditions for GOD immobilization were: 0.1% enzyme solution, immobilization temperature- 4 degrees C and immobilization time- 24 h. Immobilized GOD was applied to amperometric determination of glucose using flow-injection analysis. The optimal flow rate was determined as 4.0 ml/min when injecting 100 mu l sample volumes. The linear response range for the on-line detection of glucose using immobilized GOD in column minibioreactor was estimated to be from 0.01 mM to 20 mM (a correlation coefficient of 0.985). Moreover, its experimental detection limit is 10 mu M (S/N=3) and the apparent Michaelis-Menten constant was calculated to be 20.15 mM. The proposed method for glucose measurement was validated in real samples of fruit juices.”
“Pregnancy exposure to di(n-butyl) phthalate (DBP) in rats induces a testicular dysgenesislike syndrome (TDS) in male

offspring. Earlier studies suggested altered Sertoli cell development/maturation PRN1371 clinical trial may result, especially in testes that become cryptorchid. This study quantitatively selleck chemicals assessed Sertoli cell numerical and functional development in DISP-exposed

rats and compared (unilaterally) cryptorchid and scrotal testes. Pregnant rats were gavaged with 500 mg/kg/day DBP or corn oil from embryonic (E) Days 13.5 to 21.5. Male offspring were sampled on E21.5 or Postnatal Day 6, 10, 15, 25, or 90. Sertoli cell number in DBP-exposed males was reduced by similar to 50% at E21.5 but recovered to normal by Days 25-90, accompanied by significant changes in plasma inhibin B and testosterone levels. Sertoli cell maturational development in DBP-exposed males, assessed using five protein markers (anti-mullerian hormone, cytokeratin, androgen receptor, CDKN1B, and Nestin), was largely normal, with some evidence of delayed maturation. However, in adulthood, Sertoli cells (SC) in areas lacking germ cells (Sertoli cell-only [SCO] tubules) often exhibited immature features, especially in cryptorchid testes. Sertoli cells in DBP-exposed animals supported fewer germ cells during puberty, but this normalized in scrotal testes by adulthood. Scrotal and especially cryptorchid testes from DBP-exposed animals exhibited abnormalities (SCO tubules, focal dysgenetic areas) at all postnatal ages.