The Trans-Superior Articular Process Approach Utilizing Visual Trephine: A More Time-Saving and Effective Percutaneous Endoscopic Transforaminal Lumbar Discectomy for Migrated Lumbar Disc Herniation.

AIM: To introduce, and to evaluate the efficacy of the trans-superior articular process (trans-SAP) approach utilizing visual trephine in percutaneous endoscopic transforaminal lumbar discectomy (PETLD) for migrated lumbar disc herniation. MATERIAL AND METHODS: This study included 98 patients, 50 patients were in trans-SAP PETLD group and 48 patients were in conventional PETLD group. Visual analogue scale (VAS), Oswestry disability index (ODI), gender, age, blood loss, operation time, the frequency of X-ray fluoroscopy and the percentage of highly migrated herniation were evaluated and compared between the trans-SAP PETLD and conventional PETLD group. RESULTS: In both trans-SAP PETLD and conventional PETLD group, VAS and ODI were decreased at postoperative 1 day and 3 months compared with preoperative (p < 0.001). What's more, the VAS and ODI of postoperative 3 months were lower than postoperative 1 day (p < 0.001). There was no difference in gender, age, blood loss after the operation, and VAS during operation between trans-SAP group and conventional group (p > 0.05). The blood loss during the operation of trans-SAP group was higher (p < 0.05), but the operation time and frequency of X-ray fluoroscopy were lower than conventional group (p < 0.001). Last, trans-SAP group had a higher percentage of highly migrated herniation (p < 0.001). CONCLUSION: Both the conventional way and trans-SAP approach can achieve excellent surgical results. But, in trans-SAP group, the operation time is shorter, and X-ray fluoroscopy is less. PETLD with visual trephine has more advantages in highly migrated herniation and maybe easier to be mastered by young surgeons.

Catalytic Liquefaction of Corn Stalk under Atomosphere Prssure and the Analysis of Liquefaction Products.

With concentrated phosphoric acid as catalyst and various organic solvents as liquefying agents, corn stalk powder was liquefied into bio-oil in an autoclave, under the condition of 170 ℃. Analysis was conducted to throw light on the liquefying effects of three different agents; they are glycerol triacetate with ethylene carbonate, glycerol with ethylene carbonate and polyethylene glycol with ethylene carbonate(6∶1 ω/ω), and the properties of the biomass liquefaction oil products. FT-IR was applied to examine raw material and residues, whose chemical compositions were further analyzed with the use of GC-MS. The results of experiments indicated that the liquefaction yield of polyethylene glycol was 97.84%, the yield of glycerol triacetate was 80.20%, the yield of glycerol were36.97%. FT-IR analysis showed that the functional groups of cellulose, hemicelluloses and lignin was disappeared and liquefaction is best when polyethylene glycol with ethylene carbonate was used as the liquefaction agent. GC-MS analysis showed that the oil composition produced in this way is complex, contains organic acids and ketones, alcohols and ethers, aromatic, sugars and esters compounds.

[Spectra analysis of lignin small molecular guaiacyl coniferyl alcohol biological modification treated by laccase].

The enzymatic modification mechanism of lignin small molecular lignin guaiacyl coniferyl alcohol existing in softwood and hardwood treated by laccase was studied. Gas chromatography-mass spectrometry (GC-MS), gel permeation chromatography (GPC), FTIR spectrum and PCD(particle charge detector) etc were used for the measurement. GC-MS could not detect the coniferyl alcohol monomer after treated by laccase, so it was speculated that coniferyl alcohol participated in the reaction totally, and the structure of coniferyl alcohol was changed. GPC demonstrated that the molecular weight of coniferyl alcohol increased when it was treated by laccase, and coniferyl alcohol was polymerized. FTIR spectrum determined the reaction point of coniferyl alcohol when treated by laccase, and it is mainly phenolic hydroxyl, aromatic ring side chain substituent such as methoxy, double bound in side chain, beta-carbonyl groups, and gamma-carbonyl groups. PCD gave a result that the cationic demandv(CD) decreased by 88.38%.