Imine Bond Characterization and Properties for Controlled Release Drugs of Collagen Protein Cross-Linked Cotton Fiber

2011 ◽  
Vol 175-176 ◽  
pp. 214-219 ◽  
Author(s):  
Yun Hui Xu ◽  
Zhao Fang Du ◽  
Yu Yue Chen
Keyword(s):  
Controlled Release ◽  
Cotton Fiber ◽  
Sodium Periodate ◽  
Covalent Bond ◽  
Subsequent Treatment ◽  
Aqueous Acetic Acid ◽  
Cotton Thread ◽  
Collagen Protein ◽  
Ft Ir ◽  
Imine Bond

For exploiting the novel multifunctional ecological cotton fibers, a new cotton fiber with the collagen protein cross-linking (CPCCF) was prepared by the limited selective oxidation of a cotton thread with sodium periodate solution and subsequent treatment with a solution of collagen protein at 40°C in aqueous acetic acid. FT-IR spectra of the CPCCF suggested that the imine covalent bond between the collagen protein and the oxidized cotton fiber was formed through a series of reaction. X-ray diffractograms analysis showed that the crystallinity of oxidized cotton fiber after collagen protein treatment increased slightly. Meanwhile, Scanning electron microscopy photographs illuminated that the modification with collagen protein occurred on the surface of cotton fiber. Kjeldahl nitrogen analysis of the CPCCF showed that the maximum percentage of collagen protein introduced into cotton fiber was 1.68% (w/w). However, the breaking strength of the cotton thread oxidized partially by sodium periodate at the concentration of less than 2.0 mg ml-1 did not decrease much. Furthermore, a model experiment for the controlled release drugs was performed using aloe anthraquinone, components of a Chinese medicine, suggested potential usefulness of the CPCCF as a carrier for the controlled release drugs.

Characterization and Physical Properties of Chitosan Modified Bamboo Pulp Fiber Fabric

2011 ◽  
Vol 197-198 ◽  
pp. 1231-1235 ◽  
Author(s):  
Xin Liu ◽  
Yun Hui Xu ◽  
Wei Wei Zhang
Keyword(s):  
Controlled Release ◽  
Sodium Periodate ◽  
Raw Materials ◽  
Covalent Bond ◽  
Added Value ◽  
Aqueous Acetic Acid ◽  
Pulp Fiber ◽  
Bamboo Pulp ◽  
Recovery Angle ◽  
Fiber Fabric

With science and standard of living progressing, functional textile become more and more popular. We reported that a new bamboo pulp fiber fabric with the chitosan modification (CMBPFF) was prepared by the selective oxidation of sodium periodate and then treatment with a solution of chitosan aqueous acetic acid. The resulting CMBPFF is a nonpolluting and eco-friendly fabric product through the method of natural raw materials and no additives, which not only increase the added value of the product but also achieve natural ecological fabrics. This research using Kjeldahl nitrogen analysis showed that the maximum percentage of chitosan crosslinked on bamboo pulp fiber fabric was 10.52% (w/w). FT-IR spectra characterization suggested that the imine covalent bond between the chitosan and the oxidized bamboo pulp cellulose was formed through a series of reaction. The breaking strength of the modified fabric remained basically unchanged when the concentration of sodium periodate was less than 2.0 mg/ml. Furthermore, the chitosan modified bamboo pulp fiber fabric had the good antibacterial property. The wrinkle recovery angle and moisture regain of the chitosan modified fabric were improved. Meanwhile, a model experiment for the controlled release the drug was investigated using cactus extracts, a component of a Chinese medicine, indicated the extensive applicability of CMBPFF as a carrier for the controlled release drugs.

Crosslinking Properties on Oxidized Cotton Cellulose and Chitosan with Low Molecular Weight

2011 ◽  
Vol 332-334 ◽  
pp. 100-103
Author(s):  
Yun Hui Xu ◽  
Yong Jin Deng
Keyword(s):  
Molecular Weight ◽  
Cotton Fiber ◽  
Sodium Periodate ◽  
Periodate Oxidation ◽  
Covalent Bond ◽  
Cotton Cellulose ◽  
Cotton Fibers ◽  
Low Molecular Weight ◽  
Aqueous Acetic Acid ◽  
Xps Spectra

For exploiting green ecological cotton fiber products with the multifunction, a new cotton fiber crosslinked with chitosan of low molecular weight (CCCF) was prepared through the sodium periodate oxidation method. The reaction between amino groups of chitosan and aldehyde groups in the oxidized cotton cellulose occurred to obtain the CCCF in aqueous acetic acid solutions. The aldehyde group content in oxidized cotton cellulose increased markedly with the sodium periodate concentration, and the maximum weight gain of chitosan introduced on cotton fiber was 11.63% of the weight of cotton fibers. Furthermore, the crosslinking properties were respectively investigated by measurements of FT-IR and XPS spectra, the analysis indicated that the chitosan molecule was crosslinked on the surface of cotton fiber by the C=N covalent bond. This resulting CCCF is a novel ecological fiber and has more abilities of potential modification, which suggested useful information in planning applications for these modified cotton fibers.

Preparing Process and Properties of Collagen Modified Cotton Fiber

2011 ◽  
Vol 236-238 ◽  
pp. 1415-1419 ◽  
Author(s):  
Yun Hui Xu ◽  
Zhao Fang Du
Keyword(s):  
Cotton Fiber ◽  
Treatment Time ◽  
Ph Value ◽  
Periodate Oxidation ◽  
Aqueous Acetic Acid ◽  
Collagen Concentration ◽  
Acid Media ◽  
Xps Characterization ◽  
Aldehyde Groups

In order to develop cotton fabric underwear with the health care function, the cotton fiber was modified with the collagen (CMCF) using periodate oxidation method. The aldehyde groups on the glucose chains of the oxidized cotton cellulose were reacted with the amino groups of collagen to obtain the CMCF, and the oxidized cellulose was crosslinked with collagen in aqueous acetic acid media. The effects of collagen concentration, treatment time, reaction temperature, pH value of solution and periodate concentration on the amount of collagen crosslinked on cotton fiber were respectively discussed, and the optimal reaction technology was obtained. XPS characterization of the modified cotton fiber showed a characteristic peak about 400.0–405.0 eV corresponding to collagen, which indicated that the collagen was combined on the surface of cotton fiber. The mechanical properties of the collagen modified cotton fiber were improved. The resulting CMCF is a new natural ecological fiber and has the extensive application as a carrier for the controlled release of drugs.

Research on Crystallinity, Morphology of Cotton Subjected to Enzyme and Crosslinking Treatment

2017 ◽  
Vol 893 ◽  
pp. 71-76 ◽  
Author(s):  
Md. Nahid Pervez ◽  
Faizan Shafiq ◽  
Muhammad Munib Jilani ◽  
Zahid Sarwar ◽  
Ying Jie Cai
Keyword(s):  
Crystalline Structure ◽  
Cotton Fiber ◽  
Crystallinity Index ◽  
Cotton Fibers ◽  
Cellulose I ◽  
X Ray ◽  
Cotton Fibres ◽  
Ft Ir ◽  
Crystalline Nature ◽  
Crosslinking Agents

This paper explores the effect of prior enzymatic treatment on non-formaldehyde crosslinked cotton fiber and crystalline structure of cotton fibers after enzyme, crosslinking and a combination of enzyme and crosslinking treatments were examined by X-ray diffractometer. Results showed that during crosslinking treatment crystallinity index (%) values were increased with reduced crystallinity size and crosslinked of enzyme treated cotton did not change the crystalline nature of cotton (i.e. it was Cellulose I). In addition, by analysing FT-IR and SEM data it is confirmed that uniform presence of crosslinking agents was visible on cotton fibres.

Encapsulation and In Vitro Controlled Release of Doxycycline in Temperature-Sensitive Hydrogel Composed of Polyethyleneglycol–polypeptide (L-Alanine-co-L-Aspartate)

2021 ◽  
Vol 49 ◽  
pp. 119-129
Author(s):  
Shamo Zokhrab Tapdiqov
Keyword(s):  
Controlled Release ◽  
Correlation Coefficients ◽  
Zero Order ◽  
Temperature Sensitive ◽  
Poly Ethylene Glycol ◽  
Drug Delivery Carrier ◽  
Ft Ir ◽  
Poly Ethylene ◽  
Potential Use

Doxycycline was loaded with synthesized micelles composed of methyl Poly (ethylene glycol-block-poly (L-alanine–co–L-aspartate), or mPEG–Ala–Asp, and then characterized as a drug delivery carrier. The synthesis of the temperature-sensitive mPEG–Ala–Asp block copolymer was carried out by two-step ring-opening polymerization: firstly, the mPEG reacts with L-alanine N-carboxylic anhydride, and secondly the resulting mPEG–Ala reacts with benzyl aspartate N-carboxylic anhydride. The molecular structure of the copolymers obtained was determined by FT-IR and NMR spectroscopy methods and the micelles were characterized by SEM, TEM and DLS, respectively. The controlled release of Dox from hydrogel in the presence of PBS (8 to 9% by weight) lasts 6 to 7 days exhibiting stable release rates. The drug release mechanisms were studied: Higuchi and zero order models. The results and correlation coefficients applied to the Higuchi and zero-order models. The findings show the potential use of mPEG–Ala–Asp as an effective depot matrix to deliver anthracycline class drugs.

scholarly journals The regulatory effects of the number of VP(N-vinylpyrrolidone) function groups on macrostructure and photochromic properties of polyoxometalates/copolymer hybrid films

e-Polymers ◽  
2019 ◽  
Vol 20 (1) ◽  
pp. 1-7
Author(s):  
Zong-lai Liu ◽  
Tong-tong Yue ◽  
Wen-tian Sun ◽  
Feng-jun Zhang ◽  
Wei Feng
Keyword(s):  
Methyl Acrylate ◽  
Reduction Process ◽  
Covalent Bond ◽  
Esr Spectra ◽  
Nanocomposite Films ◽  
Hybrid Films ◽  
Photochromic Properties ◽  
Ft Ir ◽  
Regulatory Effects ◽  
Thermal Stability Of

AbstractNanocomposite films were synthesized by introducing phosphotungstic acid (PWA) into the poly (vinylpyrrolidone and methyl acrylate) (P (VP(N-vinylpyrrolidone)coMA(methyl acrylate))). FT-IR curves illustrated that non-covalent bond interaction was built between PWA particles and organic matrixes. In combination the results of SEM, TG-DTA and DSC, it was conducted that the ratio of functional groups of VP had a critical effect on the surface morphology, thermal stability of the hybrid films. Irradiated with ultraviolet light, the transparent thin hybrid films change from colorless to blue. Stored in air, the hybrid films could recover colorless gradually. The analysis of kinetics told us that higher VP content within the different systems always accompanied more superior photochromic performance, faster coloring and fading speed. Appearance of W5+ in ESR spectra indicated that the photo-reduction process between PWA and copolymer matrix occurred.

Preparation and Catalytic Performance of the Porous Polysulfone Microspheres Enabled by Immobilized Ionic Liquids for Esterification

2018 ◽  
Vol 1145 ◽  
pp. 90-94
Author(s):  
Yong Dong Zhao ◽  
Zhi Ping Zhao ◽  
Shuo Li ◽  
Peng Lu
Keyword(s):  
Ionic Liquid ◽  
Covalent Bond ◽  
Catalytic Performance ◽  
Inversion Method ◽  
Structure And Property ◽  
Porous Microspheres ◽  
H Nmr ◽  
Acidic Ionic Liquid ◽  
Ft Ir ◽  
Phase Inversion Method

Chloromethylated polysulfone (PSF-Cl) porous microspheres were prepared with non-solvent induced phase inversion method for the immobilization of acidic ionic liquid ([MIMBS][HSO4]). FT-IR, SEM, and 1H-NMR were used to characterize the structure and property of polysulfone porous microsphere supported ionic liquid (PSF-ILs). The results showed that acidic ionic liquid was supported onto the PSF-Cl porous microspheres by covalent bond. Furthermore, the catalyst exhibited a good catalytic activity with about 57% acetic acid conversion rate after 8h reaction. After the catalyst was reused for 7 times in the synthesis of ethyl acetate, the yield only decreased 6%.

3'-O-Formyl-(N-acyl)-2'-deoxyribonucleosides as building units in the synthesis of oligodeoxyribonucleotides

1982 ◽  
Vol 47 (8) ◽  
pp. 2157-2169 ◽  
Author(s):  
Jiří Smrt
Keyword(s):  
Acetic Acid ◽  
Acetic Anhydride ◽  
Thin Layer ◽  
Thin Layer Chromatography ◽  
Silica Gel ◽  
Subsequent Treatment ◽  
Aqueous Acetic Acid ◽  
Formyl Group ◽  
Layer Chromatography ◽  
Methanolic Ammonia

5'-O-Dimethoxytrityl-(N-acyl)-2'-deoxyribonucleosides afford 3'-O-formyl-(N-acyl)-2'-deoxyribonucleosides Ia-Id by the action of formic acetic anhydride followed by the action of 80% aqueous acetic acid. The formyl group is removed from Ia-Id by treatment with 1 mol l-1 triethylamine 3'-O-Formyl-2'-deoxythymidine (Ia) gives 3'-O-dimethoxytrityl-2'-deoxythymidine (V) by subsequent treatment with acetic anhydride, triethylamine, dimethoxytrityl chloride and methanolic ammonia. The use of compounds I for the synthesis of d-GGAGG (XIX) and d-T16 (XXXII) is described. Systems for thin-layer chromatography of 5'-O-dimethyltrityl-oligodeoxyribonucleotides on silica gel are described.

scholarly journals Topical Chitosan-Based Thermo-Responsive Scaffold Provides Dexketoprofen Trometamol Controlled Release for 24 h Use

Pharmaceutics ◽  
2021 ◽  
Vol 13 (12) ◽  
pp. 2100
Author(s):  
Luis Castillo-Henríquez ◽  
Pablo Sanabria-Espinoza ◽  
Brayan Murillo-Castillo ◽  
Gabriela Montes de Oca-Vásquez ◽  
Diego Batista-Menezes ◽  
...  
Keyword(s):  
Controlled Release ◽  
Kinetic Models ◽  
In Vitro Release ◽  
Solution Temperature ◽  
Burst Release ◽  
Release Studies ◽  
Dexketoprofen Trometamol ◽  
Ft Ir ◽  
Healing Wounds

Chronic and non-healing wounds demand personalized and more effective therapies for treating complications and improving patient compliance. Concerning that, this work aims to develop a suitable chitosan-based thermo-responsive scaffold to provide 24 h controlled release of Dexketoprofen trometamol (DKT). Three formulation prototypes were developed using chitosan (F1), 2:1 chitosan: PVA (F2), and 1:1 chitosan:gelatin (F3). Compatibility tests were done by DSC, TG, and FT-IR. SEM was employed to examine the morphology of the surface and inner layers from the scaffolds. In vitro release studies were performed at 32 °C and 38 °C, and the profiles were later adjusted to different kinetic models for the best formulation. F3 showed the most controlled release of DKT at 32 °C for 24 h (77.75 ± 2.72%) and reduced the burst release in the initial 6 h (40.18 ± 1.00%). The formulation exhibited a lower critical solution temperature (LCST) at 34.96 °C, and due to this phase transition, an increased release was observed at 38 °C (88.52 ± 2.07% at 12 h). The release profile for this formulation fits with Hixson–Crowell and Korsmeyer–Peppas kinetic models at both temperatures. Therefore, the developed scaffold for DKT delivery performs adequate controlled release, thereby; it can potentially overcome adherence issues and complications in wound healing applications.

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