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Lignin-containing Microfibrillated Cellulose Prepared from Corncob Residue via Calcium Hydroxide Co-grinding and Its Application in Paper Reinforcement 被引量:1
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作者 Jinghuan Chen Jingang Liu Zehong Xu 《Paper And Biomaterials》 CAS 2022年第2期37-45,共9页
In this study,lignin-containing microfibrillated cellulose(MFC)was prepared from corncob residue after xylose extraction via co-grinding with calcium hydroxide.The product was then compared with the MFC obtained by di... In this study,lignin-containing microfibrillated cellulose(MFC)was prepared from corncob residue after xylose extraction via co-grinding with calcium hydroxide.The product was then compared with the MFC obtained by direct grinding and applied to strengthen paper.The chemical composition and morphological structure analysis results showed that the corncob residue can be used to prepare lignin-containing MFC and does not require further purification.Moreover,the co-grinding with calcium hydroxide is easier to fibrillate corncob residue.The MFC obtained by cogrinding with calcium hydroxide had a higher aspect ratio,and its surface was coated with calcium carbonate nanoparticles.MFCs obtained by both the methods mentioned above had an obvious strengthening effect on paper.Compared with the paper without MFC,the tensile index,elongation,burst index,and folding strength of the paper with MFC obtained by co-grinding with calcium hydroxide significantly increased by 17.5%,22.1%,19.5%,and 157.1%,respectively.This study provides a novel idea for the utilization of corncob residue,which may enhance the value and promote the comprehensive utilization of corn by-products. 展开更多
关键词 corncob residue microfibrillated cellulose calcium hydroxide co-grinding paper reinforcement
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Nanonization of Niflumic Acid by Co-Grinding
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作者 Tímea Szunyogh Rita Ambrus Piroska Szabó-Révész 《Advances in Nanoparticles》 2013年第4期329-335,共7页
The aim of this study was to produce niflumic acid nanoparticles without using an organic solvent, in order to achieve an increased rate of dissolution of the final products. Co-grinding with excipients was used to de... The aim of this study was to produce niflumic acid nanoparticles without using an organic solvent, in order to achieve an increased rate of dissolution of the final products. Co-grinding with excipients was used to decrease the particle size. Poloxamer 188 (P) and mannitol (M) applied as co-grinding materials stabilized the system, preventing aggregation of the nanocrystals. The morphology and particle size distribution of the products were visualized by using scanning electron microscopy and laser diffraction. The crystalline states of the samples were investigated by differential scanning calorimetry and X-ray powder diffraction. The rate of dissolution of niflumic acid was measured with a paddle method from simulated media. It was concluded that the particles produced were in the nanometer range (the mean particle size was ~250 nm) and the nanoparticles maintained their crystallinity during the process. The rate of dissolution of the coground sample was significantly improved. 展开更多
关键词 Niflumic ACID PARTICLE SIZE DECREASE Nanonization co-grinding
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Evaluating the Effects of Crystallinity on Drug Release Behaviour in Itraconazole- or Miconazole-Loaded PLGA Microparticles Prepared Using a Co-Grinding Method
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作者 Kazuhiro Matsuura Honami Kojima +1 位作者 Miyako Yoshida Takahiro Uchida 《Pharmacology & Pharmacy》 2023年第9期348-362,共15页
This study aimed to prepare and characterize itraconazole (ITCZ)- or miconazole (MCZ)-loaded poly (lactide-co-glycolide) (PLGA) microparticles (MP) using a co-grinding method with ball milling, which is a solvent-free... This study aimed to prepare and characterize itraconazole (ITCZ)- or miconazole (MCZ)-loaded poly (lactide-co-glycolide) (PLGA) microparticles (MP) using a co-grinding method with ball milling, which is a solvent-free and convenient procedure. PLGA MP was prepared by grinding for 60 min, and the fixed theoretical drug loading was set at 9.1% and 16.7% for both drugs. The obtained loading efficiency for both drugs was estimated to be approximately 100%. The average diameters of the drug-loaded PLGA MP were approximately 20 - 35 μm. Powder X-ray diffraction (PXRD) or differential scanning calorimetry (DSC) confirmed amorphization of ITCZ and MCZ in ITCZ- or MCZ-loaded PLGA MP in all formulations. The drug release percentage from 9.1%-loaded ITCZ-PLGA7505 MP at 24 h was almost 50%, which was higher than that of ITCZ powder. The drug release percentage from MCZ-loaded PLGA7505 MP at 4 h was over 80%, which was higher than that of MCZ powder. This enhancement of release rate is caused by the amorphization of ITCZ or MCZ in the PLGA matrix. MCZ-loaded PLGA7510 MP showed a sustained release profile up to 24 h, suggesting that MCZ exists in an amorphous form in the PLGA matrix;however, the release rate declined owing to the large molecular weight of PLGA. Therefore, the release enhancement of antifungal drugs loaded on PLGA MP could be achieved by their amorphization using a co-grinding method with ball milling. 展开更多
关键词 co-grinding Method Ball Milling Poly (Lactide-co-Glycolide) ITRACONAZOLE MICONAZOLE Amorphization
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