• Title/Summary/Keyword: Methylcellulose

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Surface Properties and Blood Compatibility of Modified Cellulose Membrane (변성 셀룰로오즈막의 표면물성과 혈액 적합성)

  • Lee, Soon Hong;Huh, Hoon;Lee, Young Moo;Kim, Jin Il;Park, Young Hoon
    • Applied Chemistry for Engineering
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    • v.4 no.1
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    • pp.188-195
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    • 1993
  • Polyelectrolyte complexes and graft copolymers as biomaterials were synthesized from the water soluble cellulose derivatives. Polyelectrolyte complexes have been prepared from carboxymethyl cellulose (CMC) and gelatin. Graft copolymers(Mc-g-AA) were synthesized by grafting acrylic acid (AA) onto methyl cellulose(MC). (Mc-g-AA) and gelatin polyelectrolyte complexes were also prepared. The optimum conditions of each sample were investigated after chemical crosslinking or heat treatment. The preliminary results show that these materials might be interesting for biomedical applications.

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Effect of Hydrophilic-Lipophilic Balance of Drugs on Their Release Behavior from Amphiphilic Matrix

  • Yoo, Young-Tai;Shin, Hyun-Woo;Nam, Byung-Guk
    • Macromolecular Research
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    • v.11 no.4
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    • pp.283-290
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    • 2003
  • Organic drugs including aspirin, omeprazole, and naproxen with three different levels of octanol/water partition coefficient were examined for their release behavior from the amphiphilic PCL-b-PEO-b-PCL (PCEC) matrix. Scanning electron micrograph (SEM) of PCEC illustrated a well defined two-phase morphology consisted of dispersed poly(ethylene oxide) (PEO) domain and continuous polycaprolactone (PCL) phase. Differential scanning calorimetry (DSC) and X-ray diffractometry (XRD) experiments veri tied that three model drugs are dissolved as a molecular dispersion in PCEC matrix. The release of hydrophilic aspirin closely followed the water absorption profile of the matrix indicating that its major fraction is present in PEO domain. However, substantial amount of aspirin present in less hydrophilic region displayed discontinuous biphasic release pattern. In the case of omeprazole with intermediate hydrophobicity consistent release behavior was observed for a period of 24 hrs after the rapid liberation of ca. 10% of the drug presumably partitioned in PEO phase. It was ascribed to the fact that the progressive hydration of PCEC matrix gradually increased the chance of drug/water exposure to compensate the exhaustion of device. Naproxen with the highest octanol/water distribution coefficient among three model drugs exhibited a limited release of 35% for 24 hrs. Finally, hydroxypropyl methylcellulose phthalate (HPMCP)/PCEC blend matrix demonstrated an accelerated and quantitative release of hydrophobic naproxen by generating high porosity and thereby expanding polymer/water interface.

Crystal Form of Celecoxib: Preparation, Characterization and Dissolution

  • Jin, Mi-Ryung;Sohn, Young-Taek
    • Journal of the Korean Chemical Society
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    • v.62 no.5
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    • pp.352-357
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    • 2018
  • Celecoxib (4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyrazol-1-yl]benzenesulfonamide) is a cyclooxygenase-2 inhibitor used in the treatment of arthritis, acute pain, and dysmenorrhoea. Celecoxib is a Biopharmaceutics Classification System (BCS) class II compound whose oral bioavailability is highly limited owing to its poor aqueous solubility. Several polymorphs of celecoxib have been identified as Form I, Form II, and Form III with melting points of about $162.8^{\circ}C$, $161.5^{\circ}C$, and $160.8^{\circ}C$, respectively. Form IV was generated from the precipitated suspension in the presence of HPMC (Hydroxypropyl methylcellulose) and Polysorbate 80. A rapid rate of dissolution is useful because the rate of dissolution of a drug typically increases its bioavailability. The aim of this study was to investigate the possibility of production of new crystal form of celecoxib that has higher solubility than Form III. New crystal form of celecoxib (Form A) has been isolated by recrystallization and characterized by differential scanning calorimetry (DSC), thermogravimetric (TG) analysis and powder X-ray diffractometry (PXRD). Form A was dissolved faster than Form III. At 30 minutes, the dissolution of Form A was 97.3%, whereas the dissolution of Form III was 82.2% (p < 0.1). After storage of three months at $20^{\circ}C$, in 24% RH (Relative Humidity), the crystal form was not transformed.

A Comparative Analysis of Images by Changing Density and Administrative Dosage of $BaSO_4$ in the Small Bowel Series Using Methylcellulouse (Methylcellouse를 이용한 소장조영 검사시 황산바륨의 농도(%W/V)와 투여량의 변화에 따른 영상의 비교 분석)

  • Lee, Y.S.;Yoo, H.S.;Son, S.Y.;Kang, H.W.;Hong, J.B.
    • Journal of radiological science and technology
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    • v.20 no.2
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    • pp.68-72
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    • 1997
  • Small bowel series using methylcellulose are considered a better technique than using other contrast media considering a significant decrease of transit time of $BaSO_4$ and that of the necessary time for the examination. We investigated the mean transit time of $BaSO_4$, maximum luminal diamenter of small bowel, optical density and flocculation frequency after adminstratting 100 ml of 120% $BaSO_4$ to 20 pts), 150 ml of 70% $BaSO_4$ to 20 pts and 200 ml of $BaSO_4$ with 600 ml of mechylcellulose. It was shown that the technique using 150 ml of 70% $BaSO_4$ had the best result. When we apply a adequate amount of density(w/v%), dosage to pts for small bowel series using MC, we can decrease an examination time and have the better image due to double contrast. It is considered that a more study to lower the density of 70% $BaSO_4$ is necessary.

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Mechanical Properties of Rice Noodles When Adding Cellulose Ethers (셀룰로오스 에테르를 첨가한 쌀면의 기계적 물성)

  • Um, In Chul;Yoo, Young Jin
    • Current Research on Agriculture and Life Sciences
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    • v.31 no.3
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    • pp.177-181
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    • 2013
  • This study examined the effect of the molecular weight, substitution degree, and substitution type of cellulose ether on the mechanical properties of dried rice noodles. When increasing the molecular weight of the hydroxypropyl methylcellulose (HPMC), the bending strength of the dried rice noodles also increased. However, the bending strength of the rice noodles with added HPMCs was still lower than that of the wheat noodles. Meanwhile, the bending elongation of the dried rice noodles was higher than that of the wheat noodles and was increased when decreasing the molecular weight of the HPMC. In conclusion, the bending strength and elongation of dried rice noodles is affected by the substitution degree and type of cellulose ether.

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The Effects of the Different Percentages of HPMC and Enzymes on Making Rice Bread (쌀빵의 제빵 적성에 대한 HPMC와 복합 효소 첨가 수준 영향)

  • Kim, Sang Sook;Chung, Hae Young
    • Journal of the Korean Society of Food Culture
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    • v.34 no.4
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    • pp.456-462
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    • 2019
  • This study investigated the bread-making properties of rice bread supplemented with HPMC (hydroxypropyl methylcellulose) 1~3% and gluzyme (glucose oxidase), fungamyl (fungal ${\alpha}$-amylase) and pentopan (xylanase+hemicellulases) (0.0015~0.0090%). The viscoelastic properties of the dough with HPMC 1~3% were analyzed. When the rice flour was supplemented with HPMC 1~3%, the viscoelastic properties of the dough tended to increase as the amount of added HPMC was increased. The physicochemical characteristics of the rice bread with HPMC, gluzyme, fungamyl, and pentopan were analyzed. Supplementing the rice flour with HPMC, gluzyme, fungamyl, and pentopan had a significant effect on the volume (p<0.01) and specific volume (p<0.001) of the rice bread. Supplementing the rice flour with 3% HPMC and 0.0045% or 0.0090% pentopan had a significant effect on increasing the volume (p<0.01) and specific volume (p<0.001) of the rice bread. Supplementing the rice flour with 3% HPMC, 0.0023% gluzyme and 0.0015% fungamyl had a significant effect on increasing the volume (p<0.01) and specific volume (p<0.001) of the rice bread. These results suggest that supplementing the rice flour with HPMC, gluzyme, fungamyl and pentopan is effective for the production of rice bread.

Screening of Antagonistic Bacillus against Brown Rot in Dendrocalamus latiflorus and Preparation of Applying Bacterial Suspension

  • Fengying Luo;Hang Chen;Wenjian Wei;Han Liu;Youzhong Chen;Shujiang Li
    • The Plant Pathology Journal
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    • v.40 no.1
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    • pp.1-15
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    • 2024
  • The aim of this study was to isolate biocontrol bacteria that could antagonize brown rot of Dendrocalamus latiflorus, optimize the culture conditions, and develop an effective biocontrol preparation for brown rot of D. latiflorus. This study isolated a bacterium with an antagonistic effect on bamboo brown rot from healthy D. latiflorus rhizosphere soil. Morphology, molecular biology, and physiological biochemistry methods identified it as Bacillus siamensis. The following culturing media and conditions improved the inhibition effect of B. siamensis: the best culturing media were 2% sucrose, 1.5% yeast extract, and 0.7% potassium chloride; the optimal culturing time, temperature, pH, and inoculation amount were 48 h, 30℃, 6, and 20%. The optimum formula of the applying bacterial suspension was 14% sodium dodecyl benzene sulfonate emulsifier, 4% Na2HPO4·2H2O, 0.3% hydroxypropyl methylcellulose thickener, and 20% B. siamensis. The pot experiment results showed the control effect of applying bacterial suspension, diluted 1,000 times is still better than that of 24% fenbuconazole suspension. The applying bacterial suspension enables reliable control of brown rot in D. latiflorus.

Study on Korean Acid Clay as the Tablet Disintegrator (국산산성백토(國産酸性白土)의 정제붕양제(錠劑崩壤劑)로서의 개발(開發)에 관(關)한 연구(硏究))

  • Roe, Tae-Sun;Yim, Chang-Kyun
    • Journal of Pharmaceutical Investigation
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    • v.2 no.1
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    • pp.31-39
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    • 1972
  • 국산산성백토(國産酸性白土)를 정제(錠劑)의 붕노제(崩努劑)로 개발(開發)하고자 종내(從來) 붕해제(崩解劑)로 사용(使用)해 오든 corn starch, calcium methylcellulose, kaolin, calcium silicate 및 Pectin과 국산산성백토(國産酸性白土)를 붕해제(崩解劑)로하고 정제(錠劑)의 주약성분(主藥成分)으로서는 불용성(不溶性)인 Ca-PAS KP II 를 택(澤)하였다. 이상(以上)의 각(各) 붕해제(崩解劑)의 一錠當(일정당) 함양(含量)을 0%에서 25%까지 7종(種)으로 달리하고 이것을 각각(各各) 사용(使用)하여 만든 과립(顆粒)의 입자도(粒子度)도 각각(各各) 4종류(四種類)로 분류(分類)하였다. 여기에 활택제(滑澤劑) 로서 0.5% mg-stearate를 공통(共通)으로 첨가(添加)하였다. 이상(以上)을 각각(各各) 동일(同一)한 조건하(條件下)에서 타정(打錠)하여 수종(數種)의 정제(錠劑)를 만들었다. 이들 정제(錠劑)에 대(對)하여 경도(硬度)및 붕해도시험(崩解度試驗)을 하여 비교검토(比較檢討)한 결과(結果) 다음과 같은 결론(結論)을 얻었다. 1. Corn starch는 우수(優秀)한 붕해제(崩解劑)이나 그첨가량(添加量)이 8%이상(以上)이 될 때 는 타정시(打錠時) 압력(壓力)을 받지 않어 정제(錠劑) 붕해제(崩解劑)로서 사용(使用)할 수 없었다. 2. Ca-Mc는 붕해제(崩解劑)로서 첨가량(添加量)이 8%이상(以上) 일때에도 사용가능(使用可能) 하였으나 15%이상(以上) 일때는 타정시(打錠時) 압력(壓力)이 약(弱)해졌다. 3. Kaolin 붕해제(崩解劑)로서 부적당(不適當) 하다고 사려(思慮)되였다. 4. Ca-silicate도 붕해제(崩解劑)로서 적당(適當)하였으나 Pectin은 가장 부적당(不適當)하였다. 5. 산성백토(酸性白土)는 정제붕해제(錠劑崩解劑)로서 타정시(打錠時) 25% 첨가시(添加時)에도 압력(壓力)을 잘 받어 정제(錠劑)의 경도(硬度)를 유지(維持)할수 있었을 뿐만 아니라 붕해도(崩解度)도 양호(良好)한 성적(成績)을 나타내여 가장 우수(優秀)한 붕해제(崩解劑)임을 확인(確認)하였다. 6. 일반적(一般的)으로 타정(打錠)에 사용(使用)되는 과립(顆粒)의 size가 적을수륵 붕해시간(崩解時間)은 짧았으며 정제(錠劑)의 경도(硬度)가 높을수록 붕해시간(崩解時間)은 길었다. 그러나 정확(正確)한 비예성(比例性)은 찾기힘들었다.

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Preparation of Solid Dosage Form containing SMEDDS of Simvastatin by Microencapsulation (심바스타틴 자가유화약물전달시스템의 마이크로캡슐화를 통한 고형제제의 개발)

  • Kang, Bok-Ki;Yoon, Bok-Young;Seo, Kwang-Su;Jeung, Sang-Young;Kil, Hee-Joo;Khang, Gil-Son;Lee, Hai-Bang;Cho, Sun-Hang
    • Journal of Pharmaceutical Investigation
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    • v.33 no.2
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    • pp.121-127
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    • 2003
  • The objective of this study was to solidify the simvastatin self-microemulsifying drug delivery system (SMEDDS) and to improve the encapsulation efficiency of solidified alginate beads using sodium alginate. Typical simvastatin SMEDDS was composed of various oils, surfactants and cosurfactants. Also solidified-alginate beads was prepared by crosslinking liquid emulsion mixtures containing sodium alginate and other excipients (cetylpyridinum chloride (CP-Cl), hydroxypropyl methylcellulose, starch and so on). in $CaCl_2$ solution, it has been investigated that the drug release pattern and encapsulation efficiency were varied with the ratio of cationic lipid (CP-Cl). Solidified sodium alginate beads containing simvastatin SMEDDS were redispersed into media without re-aggregation. Oil droplet size of redispersed solidified-beads in media produced smaller than the initial size. The density of beads and drug loading amount were increased with increasing cationic lipid content. These systems have advantages of storage stability and predictability of drug release rate.

The Effect of Sodium Alginate Coating on the Storage Stability and Dissolution Rate of Enteric Coated Lansoprazole (알긴산 나트륨이 장용코팅된 란소프라졸 제제의 저장안정성 및 용출률에 미치는 영향에 관한 연구)

  • Kim, Jung-Hoon;Oh, Jung-Min;Khang, Gil-Son;Jeong, Je-Kyo;Lee, Jung-Sik;Jeung, Sang-Young;Lee, Hai-Bang
    • Journal of Pharmaceutical Investigation
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    • v.32 no.4
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    • pp.277-284
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    • 2002
  • Lansoprazole, pharmaceutics for acid-related diseases, is unstable in low pH environments and generally coated with enteric polymer to obtain gastroresistance in stomach. Because its storage stability is influenced by acidic substitutes of enteric polymer, alkaline chemicals wεre generally addεd to dosage form as a stabilizer. In this experience, we coated lansoprazole bead with sodium alginate and evaluated the effect of bead size and sodium alginate coating on the storage stability and dissolution profile of lansoprazole. Sodium alginate solution containing lansoprazole was sprayed as a droplet into 3% (w/v) $CaCl_2$ solution and the resultant bead was coated with starch, sodium alginate, and hydroxypropyl methylcellulose phthalate. The content of lansoprazole granule not coated with sodium alginate decreased to 57.96% of initial content when stored at a severe condition for 4 weeks, but that of lansoprazole granule coated with sodium alginate before enteric coating decreased little and as the thickness of sodium alginate film increased, the content of bead didn't decreased for 4 weeks. Sodium alginate film also improved the gastroresistance without much influencing the maximum dissolution rate.