1.The isolation and preservation of nuclei using polyethylene glycol, concanavalin A, and phytohemagglutinin.
Joo Yung KIM ; Yungchang LEE ; Kwang Yul KIM
Korean Journal of Anatomy 1992;25(1):63-70
No abstract available.
Concanavalin A*
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Polyethylene Glycols*
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Polyethylene*
2.Assessment of agnique MMF killing effect on A. sundaicus in the shrimp farms of Ca Mau province
Journal of Malaria and parasite diseases Control 2004;0(3):56-56
Insecticidal effects of Agnique MMF were investigated in the coastal brackish water shrimp farms in the Tan Thuan commune, Dam Doi district of Ca Mau province in 2000. The investigations were made in terracotta jars and shrimp ponds with the surface area 30m2 and 1000m2 each. Agnique MMF was found to have a high and fast killing effect on larvae of An.sundaicus at all three testing doses of 0.3ml/m2, 0.4ml/m2 and 0.5ml/m2. Especially larvae at instars of III, IV and pupae. However, the insecticide produced a low effect on Culex sitiens killing larvae of IV ins tar and only retarding larvae of I, II, III instar. The residual effect of Agnique MMF was found to be 14 days in the terracotta jars and 6 days in the ponds. In the direct observations, Agnique MMF was found to have no negative effects on rearing shrimps
Fatty Alcohols
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Polyethylene Glycols
3.Enhanced bioavailability of total paeony glycoside by self-microemulsifying drug delivery system.
Li-Jiang CHEN ; Yang LIU ; Yu LIU ; Li LI ; Fei GAO
Acta Pharmaceutica Sinica 2012;47(12):1678-1686
Total paeony glycoside (TPG) is extracted and purified from a traditional Chinese herbal medicine. It has many biological and pharmacological activities. However, there are few dosage forms of TPG in the market because of its low bioavailability. Self-microemulsifying drug delivery system (SMEDDS) is a vital tool in solving low bioavailability of poor absorption drugs. So the objective of this study is to develop a new TPG-SMEDDS for the oral delivery of poorly soluble TPG. Through the construction of pseudo-ternary phase diagrams, the optimum prescription was obtained, which consisted of 18.70% TPG, 16.27% ethyl oleate as oil, 43.34% Cremophor RH40 as surfactant and 21.73% Transcutol P as cosurfactant. The characterizations of TPG-SMEDDS including morphological characterization, droplet size, zeta-potential, emulsification time, and dissolution study of TPG-SMEDDS were evaluated. The results showed that TPG-SMEDDS is stable and its release rate is high in four different media (0.1 mol x L(-1) HCl, pH 6.8 PBS, pH 7.4 PBS, and water). The relative bioavailability of SMEDDS was dramatically enhanced in an average of 1.52-fold that of TPG-suspension. It is concluded that the bioavailability of TPG is enhanced greatly by SMEDDS.
Administration, Oral
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Animals
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Biological Availability
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Drug Delivery Systems
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Drug Stability
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Emulsions
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Ethylene Glycols
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chemistry
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Glycosides
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administration & dosage
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chemistry
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isolation & purification
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pharmacokinetics
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Oleic Acids
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chemistry
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Paeonia
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chemistry
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Particle Size
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Pharmaceutical Vehicles
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chemistry
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Plants, Medicinal
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chemistry
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Polyethylene Glycols
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chemistry
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Rats
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Solubility
4.Mechanisms of hydroxypropyl methylcellulose for the precipitation inhibitor of supersaturatable self-emulsifying drug delivery systems.
Acta Pharmaceutica Sinica 2013;48(5):767-772
Hydroxypropyl methylcellulose (HPMC) propels self-emulsifying drug delivery systems (SEDDS) to achieve the supersaturated state in gastrointestinal tract, which possesses important significance to enhance oral absorption for poorly water-soluble drugs. This study investigated capacities and mechanisms of HPMC with different viscosities (K4M, K15M and K100M) to inhibit drug precipitation of SEDDS in the simulated gastrointestinal tract environment in vitro. The results showed that HPMC inhibited drug precipitation during the dispersion of SEDDS under gastric conditions by inhibiting the formation of crystal nucleus and the growth of crystals. HPMC had evident effects on the rate of SEDDS lipolysis and benefited the distribution of drug molecules across into the aqueous phase and the decrease of drug sediment. The mechanisms were related to the formed network of HPMC and its viscosities and molecular weight. These results offered a reference for selecting appropriate type of HPMC as the precipitation inhibitor of supersaturatable SEDDS.
Caprylates
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chemistry
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Chemical Precipitation
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drug effects
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Crystallization
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Drug Delivery Systems
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methods
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Emulsifying Agents
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chemistry
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Emulsions
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Ethylene Glycols
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chemistry
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Glycerides
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chemistry
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Hypromellose Derivatives
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administration & dosage
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chemistry
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pharmacology
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Indomethacin
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administration & dosage
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chemistry
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Lipolysis
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drug effects
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Molecular Weight
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Polyethylene Glycols
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chemistry
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Viscosity
5.Effect of three penetration enhancers on corneal permeability of mangiferin in vitro.
Rui LIU ; Zhidong LIU ; Lexin SHU ; Chengui ZHANG ; Boli ZHANG
China Journal of Chinese Materia Medica 2010;35(23):3131-3135
OBJECTIVETo investigate the effects of labrasol, solutol HS 15 and transcutol P on the corneal permeability of mangiferin in vitro.
METHODThe effects of three penetration enhancers on the corneal permeability of mangiferin were investigated in vitro by using isolated rabbit corneas.
RESULTThe apparent Papp enhancements were increased 1.80, 3.27, 3.41 and 4.76-folds with Lab at 1.0%, 1.5%, 2.0% and 3.0% (P < 0.01), respectively. The apparent Papp increased 1.98 and 3.07-folds with Sol at 0.2% and 0.4% (P < 0.01), respectively, but reduced with 0.010%-0.03% Trans.
CONCLUSIONThe Papp value of mangiferin is significantly enhanced by 1.0%-3.0% Lab, 0.2% and 0.4% Sol, however the Papp value of mangiferin is reduced by 0.01%-0.03% Trans.
Animals ; Cornea ; drug effects ; metabolism ; Drug Carriers ; chemistry ; Ethylene Glycols ; chemistry ; Glycerides ; In Vitro Techniques ; Organic Chemicals ; chemistry ; Permeability ; Plant Extracts ; pharmacokinetics ; Polyethylene Glycols ; chemistry ; Rabbits ; Stearic Acids ; chemistry ; Xanthones ; pharmacokinetics
6.Synthesis, characterization and blood compatibility studies of waterproof breathable polyurethanes.
Peng WANG ; Jianbin LUO ; Minhui DU ; Chengsheng HE ; Cuirong FAN ; Yinping ZHONG
Journal of Biomedical Engineering 2005;22(4):734-738
Adopting the two-step method and changing the proportion between PEG (Polyethylene glycol) and PTMG (poly (tetrahydrofuran), we used the MDI (4,4'-diphenylmethane diisocyanate) and short chain extender BDO (1,4-butanediol) as hard segment, the PTMG and PEG as soft segment, and hence prepared a series of polyether-based thermoplastic polyurethanes. FTIR showed the structure character of these polyurethanes. The determination of mechanics property and water contact angles revealed their good mechanics properties and hydrophilicity. Blood compatibility was evaluated by hemolysis test and platelet adhesion test, which revealed their good hemocompatibility. So those polyurethanes may be of wide application in the future.
Animals
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Biocompatible Materials
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chemical synthesis
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chemistry
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Butylene Glycols
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chemistry
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Isocyanates
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chemistry
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Materials Testing
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Polyethylene Glycols
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chemistry
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Polymers
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chemistry
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Polyurethanes
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chemical synthesis
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chemistry
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Rabbits
7.Unusually Elevated Serum Insulin Level in a Diabetic Patient during Recombinant Insulin Therapy.
Serim KIM ; Yeo Min YUN ; Mina HUR ; Hee Won MOON
Laboratory Medicine Online 2013;3(1):56-59
Herein, we report a case of unusually elevated serum insulin level as a result of increased anti-insulin antibody (IA)-bound insulin after continuous subcutaneous insulin infusion therapy. Detecting free insulin (unbound IAs) levels after polyethylene glycol pre-treatment could be useful to assess functional insulin levels in diabetic patients receiving insulin therapy. The E170 insulin assay can estimate total insulin (bound IAs and free insulin) levels, but it does not measure the levels of exogenous insulin analogues.
Humans
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Insulin
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Insulin Antibodies
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Polyethylene Glycols
9.Remarks on the effectiveness of hypertonic saline-epinephrine solution and polidocanol solution in the treatment of bleeding peptic ulcer
Journal of Practical Medicine 2005;510(4):23-25
Prospective study on 107 bleeding peptic ulcer patients treated at Hospital No 103 from July 2001 to December 2002. Participants were divided into 2 groups. Group 1 received hemostatic therapy with polidocanol solution (PLS). Group 2 were treated by hypertonic saline-epinephrine (HSE) solution. Results: The general rate of successful hemostasis was 96.3%, in PLS group was 92.3% and in HSE group was 100%. There were not differences in the rates of initial hemostasis between 2 groups (p>0.05). Hemostatic effect was achieved after the first injection in 76.9% (40 patients) of PLS group and in 85.5% (47 patients) of HSE group. Some patients needed 2nd injections (PLS group: 15.4%, HSE group: 3.7%). Both solutions were effective in the treatment of bleeding peptic ulcer. HSE solution is safe, simple, low cost, and appropriate in Vietnam.
Peptic Ulcer
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Therapeutics
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Epinephrine
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Polyethylene Glycols
10.Low Volume Polyethylene Glycol (PEG) Plus Ascorbic Acid, a Valid Alternative to Standard PEG.
Gut and Liver 2016;10(2):160-161
No abstract available.
*Ascorbic Acid
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Cathartics
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Colonoscopy
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Humans
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*Polyethylene Glycols