UV-vis spectroscopic detection of formaldehyde and its analogs: A convenient and sensitive methodology.

Formaldehyde is deemed to be an indispensable industrial product that has been widely applied in manufacture of resins, drugs, building materials, etc. It has been widely accepted that, nevertheless, residual formaldehyde will cause pathogen reactions, even leading to cancers like leukemia. Thus, a facile and efficient approach has been designed to achieve the determination of formaldehyde by ultraviolet and visible (UV-vis) spectrophotometry in liquid media. In detail, O-(carboxymethyl) hydroxylamine (C2H5NO3·0.5HCl) is chosen as the detection reagent for the specific recognition of formaldehyde on account of its unique aminooxy (-O-NH2) which can react with formaldehyde to form oxime bonds (O-NCH2), accompanied with the only by-product of H2O. Likewise, this simple and sensitive detection approach based on the chemical detection reagent C2H5NO3·0.5HCl can also be applied to the determination of other aldehyde homologs with carbonyl groups including acetaldehyde, acetone, benzaldehyde, 1, 4-phthalaldehyde. As a result, all the UV absorbances of analytes display remarkable linear detection relationships. The limits of detection (LOD) and limits of quantitation (LOQ) values are in the range of 0.03-1.16 ppm and 0.03-5.81 ppm respectively, with RSDs of 3.27-3.75 %, evidencing the feasibility of our method to determine formaldehyde and its homologs by UV-vis spectrophotometry and auspicious prospects of practical applications.

Endogenous CBS-H2S Pathway Contributes to the Development of CCI-Induced Neuropathic Pain.

Studies showed a complex relationship between hydrogen sulfide (H2S) and neuropathic pain. In this study, the relationship between endogenous CBS-H2S pathway in L4-6 spinal cord and neuropathic pain was explored. A total of 163 adult Kunming mice were used in this study. CBS expression and H2S formation in L4-6 spinal cord were detected in the development of neuropathic pain firstly. Then, effect of AOAA, an CBS inhibitor, on treatment of neuropathic pain by chronic construction injury surgery (CCI) was detected. Pain thresholds and activation of NF-κB(p65), ERK1/2 and CREB were measured as biomarks of neuropathic pain. Results showed that CCI surgery significantly upregulated protein expression of CBS and H2S formation. Correlation analysis showed pain thresholds had negative relationships with protein expression of CBS and H2S formation. Treatment with AOAA, a CBS inhibitor, inhibited CCI-induced upregulation of CBS expression and H2S formation (P < 0.05). Further, AOAA significantly decreased activation of NF-κB(p65), ERK1/2 and CREB pathway, and reversed CCI-induced allodynia (P < 0.05). This indicated that CBS-H2S pathway promoted the development of neuropathic pain. CBS-H2S pathway could be a promising target for treatment of neuropathic pain.