1.Histopathological changes of testes and eyes by neutron irradiation with boron compounds in mice.
Yeon Joo KIM ; Won Ki YOON ; SI Yun RYU ; Ki Jung CHUN ; Hwa Young SON ; Sung Whan CHO
Journal of Veterinary Science 2006;7(1):19-23
This study was performed to investigate the biological effects of boron neutron capture therapy (BNCT) on the testes and eyes in mice using HANARO Nuclear Reactor, Korea Atomic Energy Research Institute. BNCT relies on the high capacity of (10)B in capturing thermal neutrons. Sodium borocaptate (BSH, 75 ppm, iv) and boronophenylalanine (BPA, 750 ppm, ip) have been used as the boron delivery agents. Mice were irradiated with neutron (flux: 1.036739E +09, Fluence 9.600200E+12) by lying flat pose for 30 (10 Gy) or 100 min (33 Gy) with or without boron carrier treatment. In 45 days of irradiation, histopathological changes of the testes and eyes were examined. Thirty-three Gy neutron irradiation for 100 min induced testicular atrophy in which some of seminiferous tubules showed complete depletion of spermatogenic germ cells. Lens epithelial cells and lens fiber were swollen and showed granular changes in an exposure time dependent manner. However, boron carrier treatment had no significant effect on the lesions. These results suggest that the examination of histopathological changes of lens and testis can be used as "biological dosimeters" for gauging radiation responses and the HANARO Nuclear Reactor has sufficient capacities for the BNCT.
Animals
;
Boranes/*pharmacology
;
Borohydrides/*pharmacology
;
Boron Neutron Capture Therapy/*methods
;
Eye/pathology/*radiation effects
;
Histocytochemistry
;
Male
;
Mice
;
Mice, Inbred C57BL
;
Neutrons
;
Phenylalanine/*analogs&derivatives/pharmacology
;
Seminiferous Tubules/pathology/*radiation effects
;
Specific Pathogen-Free Organisms
;
Sulfhydryl Compounds/*pharmacology
2.Characterization of chemical components of essential oil from flowers of Chrysanthemum morifolium produced in Anhui province.
Ya-Jun WANG ; Qiao-Sheng GUO ; Xiu-Wei YANG ; Wen-Bin XU ; Hai-Yan TAO
China Journal of Chinese Materia Medica 2008;33(19):2207-2211
OBJECTIVETo analyze the chemical components of the essential oil extracted from six cultivars' Juhua (Zaogongju, Wangongju, Huangyaoju, Chuju, Xiaoboju and Daboju) produced in Anhui province of China, which were breed from Chrysanthemum morifolium, and to provide scientific basis for quality control.
METHODThe essential oils of the six cultivars'Juhua were extracted by water-steam distillation and separated by GC capillary column chromatography. The components were quantitatively determined with normalization method, and identified by GC-MS.
RESULTFrom Zaogongju, Wangongju, Huangyaoju, Chuju, Xiaoboju and Daboju, 247, 226, 246, 182, 216 and 122 chromatographic peaks were detected, among them 75, 54, 78, 50, 53 and 43 components were identified,which were composed of 85.67%, 82.80%, 81.38%, 73.22%, 71.51% and 72.87% of the total essential oil, respectively.
CONCLUSIONMonoterpenoid compounds were higher more than sesquiterpenoid compounds in the five juhua except for Chuju. There was no difference in the constituents of essential oil of Zaogongju and Wangongju. And verbenyl acetate was the main chemical constituent and composed of 32.10% and 37.85% of the total essential oil, respectively. (1R)-Camphor and bisabolol oxide A were the main chemical constituents in Huangyaoju, which were composed of 28.70% and 12.58% of the total essential oil, respectively. beta-Selinene and borneol were the main chemical constituents in Chuju, which were composed of 17.85% and 12.84% of the total essential oil, respectively. Eucalyptol was the main chemical constituent in Xiaoboju, which were composed of 21.33%. Verbene oxides and chrysanthenone were composed of 25.32% and 8.26% of the total essential oil, respectively, in the Daboju. The common chemical constituents were camphene, borneol, bornyl aceate, (1R)-camphor, (-)-4-terpineol, alpha-terpineol, eucalyptol, cis-caryophyllene, caryophyllene oxide, juniper camphor, beta-sesquiphellandrene, alpha-curcumene and beta-farnesene in the six cultivars' Juhua produced in Anhui province of China. The resultant data provided the further evidences to distinguish Juhua' cultivars and scientific basis for quality control of Juhua.
Boranes ; chemistry ; Bornanes ; chemistry ; Camphor ; chemistry ; China ; Chrysanthemum ; chemistry ; Cyclohexanols ; chemistry ; Gas Chromatography-Mass Spectrometry ; Monoterpenes ; chemistry ; Oils, Volatile ; chemistry ; Sesquiterpenes ; chemistry ; Terpenes ; chemistry ; Tetrahydronaphthalenes ; chemistry
3.Synthesis and antiproliferative activities of novel 5'-Schiff-base group substituted psoralen derivatives.
Chao-Yue CHEN ; Jian-Guo SUN ; Zhi-Zhen HUANG ; Tim-Tak KWOK ; Kwok-Pui FUNG ; Ping WU ; Fei-Yan LIU
Acta Pharmaceutica Sinica 2011;46(1):64-69
It was found that psoralen derivative could perform a Friedel-Crafts acylation smoothly with acetic anhydride to give 5'-acetylpsoralen in a 73% yield. In the presence of boron trifluoride etherate, 5'-acetylpsoralen reacted with both aromatic amines and aliphatic amine smoothly to afford 5'-Schiff-base group substituted psoralen derivatives in 72%-92% yields. The novel synthetic method has the advantages of cheap materials, mild reaction conditions, good yields and high regioselectivity in the Friedel-Crafts acylation. Cell viability assay by MTT demonstrates that some of the psoralen derivatives 6 have antiproliferative activities.
Acylation
;
Boranes
;
chemistry
;
Cell Line, Tumor
;
Cell Proliferation
;
drug effects
;
Furocoumarins
;
chemical synthesis
;
chemistry
;
pharmacology
;
Humans
;
Molecular Structure
;
Schiff Bases
;
chemistry
4.Resonance Rayleigh scattering spectra of berberine-tetraphenylboron association nanoparticle and its analytical application.
Jie-ming ZOU ; Hong-liu JIANG ; Li-sheng WANG ; Zhi-liang JIANG
Acta Pharmaceutica Sinica 2003;38(7):530-533
AIMTo study the relationship between resonance Rayleigh scattering(RRS) and the formation of association nanoparticle, and to develop a new and sensitive RRS method for the determination of trace berberine (BB).
METHODSThe association nanoparticle between BB and tetraphenylboron (TPB) was investigated by means of RRS, absorption spectral method and transmission electron microscope (TEM).
RESULTSIn pH 5.0 NaAc-HAc buffer solution, BB and TPB combine to BB-TPB association complex. The association complexes aggregate to (BB-TPB)n association nanoparticles, due to the strong hydrophobic force and Van der Waals force. It exhibits a resonance Rayleigh scattering peak at 470 nm, a maximum absorption peak at 368 nm. A new RRS method was proposed for the determination of 0.06 to 5.28 mg.L-1 BB in real samples with satisfactory results. The detection limit is 26 micrograms.L-1.
CONCLUSIONThe TEM of (BBjAgp-TPBj + p)h composite association nanoparticles was observed by means of composite association nanoreaction both TPB- and BB+ or Ag+. The results indicated that the formation of (BB-TPB)n association nanoparticles and interface of solid-liquid results in the enhanced resonance light-scattering. This new RRS method showed high sensitivity, and had been successfully applied to the determination of BB in real samples.
Berberine ; administration & dosage ; analysis ; Drug Carriers ; Drugs, Chinese Herbal ; administration & dosage ; analysis ; Nanotechnology ; Scattering, Radiation ; Spectrum Analysis ; Tablets ; Technology, Pharmaceutical ; methods ; Tetraphenylborate ; chemistry
5.Determination of diborane in the air of workplace by ICP-AES.
Chun-Guang DING ; Jing ZHANG ; Hui-Fang YAN
Chinese Journal of Industrial Hygiene and Occupational Diseases 2011;29(6):452-454
OBJECTIVEA sampling method was established to collect diborane in the air of workplace and an ICP-AES method was developed to determine the Boron in desorbed solution.
METHODDiborane in the air of workplace was collected by solid sorbent tube filled with oxidant impregnated activated carbon. The adsorbed diborane was desorbed into 3% H2O2 aqueous, and then the desorbed Boron was determined by ICP-AES.
RESULTSThe sampling efficiency of this method was 99.6% with the desorption efficiency of diborane with 5.660 microg and 56.6 microg spiked were 90.9% and 99.5%, respectively. Both the intra-and inter-precision RSD were less than 8%. The standard curve of this method ranged from 0.1 to 10.0 microg/ml (Boron), and the LOD and LOQ were 0.011 mg/m3 and 0.035 mg/m3 (15L samples) respectively.
CONCLUSIONThe method established was suitable for diborane sampling and determination in the air of workplace.
Air Pollutants, Occupational ; analysis ; Borohydrides ; analysis ; Environmental Monitoring ; methods ; Spectrophotometry, Atomic ; methods ; Workplace
6.Analysis of paraquat in blood and urine by sodium borohydride/nickel chloride chemical reduction-gas chromatography/thermionic specific detector.
Lu-Yao HUANG ; Lin-chuan LIAO ; Li-Li CHEN ; Gui SU ; Wen-Jia LI ; Rong HE ; You-Yi YAN ; Lin YANG
Journal of Forensic Medicine 2008;24(6):429-432
OBJECTIVE:
To establish a new method for the analysis of paraquat in blood and urine by sodium borohydride/nickel chloride chemical reduction-gas chromatography/thermionic specific detector.
METHODS:
An initial procedure of precipitation was performed by adding hydrochloric solution with sodium chloride and a mixture of chloroform and ethanol. Then the analyte contained in supernatant was reduced by a reduction system of sodium borohydride and nickel chloride and extracted by acetic ether. Ethyl paraquat (EPQ) was used as internal standard. GC/TSD was used to identify and quantify the analyte.
RESULTS:
The limits of detection (S/N=3) in blood and urine were 0.002 and 0.004 microg/mL, respectively. The linear ranges were 0.050-30.0 microg/mL. Correlation coefficients in blood and urine were 0.999 and 0.998, respectively. The recoveries exceeded 80% both in blood and urine.
CONCLUSION
This method is applicable for quantification of paraquat in biological fluids.
Borohydrides/chemistry*
;
Chromatography, Gas/methods*
;
Forensic Toxicology
;
Herbicides/urine*
;
Humans
;
Nickel/chemistry*
;
Oxidation-Reduction
;
Paraquat/urine*
;
Sensitivity and Specificity