复方单硝酸异山梨酯-阿司匹林双缓释微丸胶囊的研制(Ⅱ)

以乙基纤维素、丙烯酸树脂Ⅱ和丙烯酸树脂Ⅲ为骨架材料分别制备单硝酸异山梨酯和阿司匹林混合骨架缓释微丸，并通过包薄膜衣进一步控制药物的释放。通过测定微丸的释放度对处方工艺进行评价，选择最佳微丸灌装胶囊．胶囊中两种药物均达到良好的缓释效果。符合中国药典对缓释制剂的要求．其体外释放过程同时符合Higuchi方程和一级释药方程，R^2值均在0．995以上。     

New polymer syntheses. LXXXII. Syntheses of poly(ether-sulfone)s from silylated aliphatic diols including chiral monomers

Attempts were made to synthesize poly(ether-sulfone)s from aliphatic diols or bissilylated diols on the one hand, and 4,4′-dichlorodiphenylsulfone or 4,4′-difluorodiphenylsulfone on the other hand. The reaction conditions and the catalyst were varied. Polycondensations of silylated diols with 4,4′-difluorodiphenylsulfone and powdered K₂ CO₃ in N-methylpyr-rolidone proved to give the best results. Using silylated isosorbide and isomannide as mono-mers chiral poly(ether-sulfone)s were prepared. GPC measurements indicate weight-average molecular weights in the range of 27×10³–200×10³. © 1995 John Wiley & Sons, Inc.     

Waterborne polyesters partially based on renewable resources

A new experimental approach for preparing biobased, water‐soluble polyesters (PEs) via titanium(IV) n‐butoxide‐catalyzed bulk polycondensation is presented. In the described method polymers were obtained from isosorbide, maleic anhydride and poly(ethylene glycol) (PEG). The chemical structure of the synthesized PEs was confirmed using 2D NMR spectroscopy and by titration methods. Careful analysis of 2D NMR spectra viz. correlation spectra (COSY), heteronuclear single quantum correlation spectra (HSQC) and heteronuclear multiple‐bond correlation spectra (HMBC) allowed to accomplish the complete proton assignment of isosorbide, PEG, and unsaturated acid residues in the PEs. Moreover, by using NMR spectroscopy the transformation of maleic anhydride into fumaric acid ester and the absence of maleic acid ester units in the final polymer were proven. However, during polycondensation part of the unsaturated bonds has reacted in a Michael addition with isosorbide or PEG. Gel permeation chromatography measurements revealed that the unsaturated PEs have M_n values in the range 3000–5000 g/mol. These PEs, with a low content of carboxylic acid end groups, exhibited sufficient thermal resistance for practical applications, for example, as free radical curable coatings. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010     

Polyterephthalates made from Ethylene glycol, 1,4‐cyclohexanedimethanol,and isosorbide

Three series of terephthalate polyesters (copolyesters and terpolyesters) containing 70, 80, and 90 mol % of ethylene glycol respectively, 1,4‐cyclohexanedimethanol (CHDM) and isosorbide in varying ratios, were synthesized by melt polycondensation. It was found that only ～75 mol % of the feeding isosorbide was incorporated in the resulting polyesters and that their content in diethylene glycol oscillated between 2 and 4 mol %. The polyesters had weight‐average molecular weights in the 25,000–33,000 g mol^?1 range and polydispersities between 2 and 2.5. The combined ¹H and ¹³C NMR analysis revealed that the microstructure of all these polyesters was at random. They showed good thermal stability with decomposition temperatures above 400 °C. Their glass‐transition temperatures were observed to increase with the content in cyclic diols, this effect being more pronounced when isosorbide was the replacing comonomer. Only the series containing 90 mol % of ethylene terephthalate units was able to crystallize upon cooling from the melt. Compared isothermal crystallizations revealed that isosorbide was more effective than CHDM in repressing the crystallizability of PET. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011     

Unsaturated,biobased polyesters and their cross‐linking via radical copolymerization

Biobased, unsaturated polyesters derived from isosorbide, maleic anhydride, and succinic acid were synthesized and characterized. The presence of maleic anhydride units in the structure of the polyesters allowed converting them into cured coatings by radical copolymerization with crosslinking agents such as 2‐hydroxyethyl methacrylate, N‐vinyl‐2‐pyrrolidinone, acrylic acid or methacrylamide. The investigated polyesters were obtained via bulk polycondensation, catalyzed by titanium(IV) n‐butoxide. 2D NMR and MALDI‐Tof‐MS spectroscopy proved that this polymerization resulted in isomerization of maleic acid units into fumaric ones and in the formation of slightly branched structures by the reaction of isosorbide (end) groups with main chain unsaturated bonds. Moreover, some double bonds proved to have reacted with the condensation by‐product water. The resulting polyesters displayed the expected correlation between variables such as molecular weight and content of unsaturated bonds and their T_g values. Since the thermal properties of the obtained polyesters were appropriate for coating applications, the polymers were crosslinked with unsaturated monomers by radical copolymerization. The crosslinking process was studied using FTIR spectroscopy and by measurements of the soluble part of the cured coatings. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 48: 2885–2895, 2010     

Isosorbide‐based polysebacates as polymeric components for development of in situ forming implants

In situ forming implants (ISFIs) appear to be a convenient drug delivery system, alternative to conventional preformed implants and microparticles for parenteral drug delivery applications. It has been shown that they offer several advantages including easy and minimally invasive application, potential for local/site‐specific drug delivery that allows reduction of side effects associated with systemic administration of drug. A few ISFI formulations based on poly(α‐hydroxy acids), solidifying by solid phase separation, are currently commercially available. In this work, polyesters based on sebacic acid, isosorbide, and optionally 1,2‐propanediol were synthesized and characterized. Poly(isosorbide sebacate‐co‐1,2‐propylene sebacate) (PISEBPG) was chosen as an essential constituent of new ISFI formulations dedicated to controlled release of doxycycline hyclate (DOXY). Basic characteristics of new ISFI formulations were investigated. In particular, the influence of addition of a relatively hydrophobic cosolvent (triacetin, TA) to a more hydrophilic 1‐methyl‐2‐pyrrolidone (NMP) as well as the presence of calcium carbonate (CAC) on the morphology of resulted depots and DOXY release profile was evaluated. Scanning electron microscopy (SEM) analysis revealed that the presence of TA resulted in more porous morphology of the depots. DOXY has been releasing continuously from depots in vitro within 12 weeks depending on the composition. The release profile of the PISEBPG‐based formulation containing CAC indicates that it could be useful where short‐term (up to 14 d), rapid release of the antibiotic is required, while formulation without CAC, where after 21 days about 50% of the drug loaded may still be available for release, may be better for the long‐term delivery of DOXY.     

Polymers of carbonic acid. XXIV. Photoreactive,nematic or cholesteric polycarbonates derived from hydroquinone-4-hydroxybenzoate 4,4′-dihydroxychalcone and isosorbide

Numerous polycarbonates were prepared by means of “diphosgene” in pyridine using hydroquinone 4-hydroxybenzoate (HQHB) as mesogenic diphenol. In addition to the homopolycarbonate, binary copolycarbonates of HQHB and 4,4′-dihydroxychalcone (DHC) with varying molar composition were prepared. A series of ternary copolycarbonates were obtained by incorporation of isosorbide. Furthermore, an alternating copolycarbonate of HQHB and isosorbide was synthesized. All polycarbonates were characterized by inherent viscosities, elemental analyses, IR-, ¹H-NMR, and ¹³C NMR spectroscopy, by WAXS powder patterns DSC measurements, and optical microscopy with crossed polarizers. The homopolycarbonate of HQHB and most binary copolycarbonates were semicrystalline materials forming an enantiotropic nematic melt. Particularly noteworthy is the finding that the alternating copolycarbonate of HQHB and isosorbide forms a broad cholesteric phase despite the unfavorable stereochemistry of isosorbide. The ternary copolycarbonates containing isosorbide formed a cholesteric melt and a Grandjean texture upon shearing. © 1997 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 35 : 1611–1619, 1997     

New polymers of carbonic acid. XXV. Photoreactive cholesteric polycarbonates derived from 2,5‐bis(4′‐hydroxybenzylidene)cyclopentanone and isosorbide

Several binary copolycarbonates were prepared by polycondensation of 2,5‐bis(4‐hydroxybenzylidene)cyclopentanone, BHBC, with methylhydroquinone, MHQ, hydroquinone 4‐hydroxybenzoate, HQHB, or isosorbide. Furthermore, five ternary copolycarbonates were prepared based on the aforementioned monomers. All polycondensations were conducted in pyridine with trichloromethyl chloroformate as condensing agent. All polycarbonates were characterized by elemental analyses, viscosity and DSC measurements, IR and ¹H‐ and ¹³C‐NMR spectroscopy, optical microscopy, and the WAXS powder pattern. All isosorbides containing binary and ternary copolycarbonates were found to form a cholesteric melt, but only three of them were capable to form a stable Grandjean texture upon shearing. © 1999 John Wiley & Sons, Inc. J Polym Sci A: Polym Chem 37: 1125–1133, 1999     

Synthesis and characterization of isomeric diphenylphosphatoisosorbide acrylates

Abstract

Isosorbide is a diether diol readily available from starch, an abundant, renewable biomaterial. Because of its structure and functionality, it may serve as a base for the development of nontoxic polymer additives, particularly flame retardants. Conversion of one of the hydroxyl groups to a diphenylphosphato moiety followed by conversion of the other to an acrylate affords isomeric vinyl monomers suitable for copolymerization with a variety of monomers to generate flame-retardant polymers.     

Copolycarbonates of isosorbide and various diols

Isosorbide and equimolar amounts of various diols were polycondensed with diphosgene and pyridine. Bisphenol A, 3,3′‐dimethyl bisphenol A, bisphenol C, 1,3‐bis(4‐hydroxybenzoyloxy)propane, and 1,4‐cyclohexane diol were used as comonomers. The compositions were determined by ¹H NMR spectroscopy; the random sequences were characterized by ¹³C NMR spectroscopy. For the high‐molar‐mass copolycarbonates of bisphenol A, 3,3′‐dimethyl bisphenol A, and bisphenol C, matrix‐assisted laser desorption/ionization time‐of‐flight mass spectrometry proved that the chain growth was mainly limited by cyclization. Copolycarbonates with alternating sequences were obtained by the polycondensation of bisphenol A with isosorbide bischloroformiate or from isosorbide and bisphenol A bischloroformiate. In these cases, large amounts of cyclic oligo‐ and polycarbonates were also formed. The glass‐transition temperatures were determined by differential scanning calorimetry measurements. © 2006 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 44: 3616–3628, 2006