• Journal of Pharmaceutical Investigation
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• 제35권2호
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• pp.95-99
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• 2005

Mucoadhesive microspheres were prepared by interpolymer complexation of chitosan with poly(acrylic acid) (PAA) and solvent evaporation method to increase gastric residence time. The chitosan-PAA complex formation was confirmed by differential scanning calorimetry and swelling study. The DSC thermogram of chitosan-PAA microspheres showed two exothermic peaks for the decomposition of chitosan and PAA. The swelling ratio of the chitosan-PAA microspheres was dependent on the pH of the medium. The swelling ratio was higher at pH 2.0 than at neutral pH. The results indicated that the microspheres were formed by electrostatic interaction between the carboxyl groups of PAA and the amine groups of chitosan. The effect of various process parameters on the formation and morphology of microspheres was investigated. The best microspheres were obtained when 1.5% of the high molecular weight chitosan and 0.3% of PAA were used as an internal phase. The optimum internal phase volume was 7%. The com oil was used as the external phase of emulsion, and span 80 was used as the surfactant. The prepared microspheres had spherical shape.

• Journal of Pharmaceutical Investigation
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• 제36권3호
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• pp.175-184
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• 2006

Poly(D,L-lacic acid)(PLA) microshperes containing loazepam were prepared by a solvent-emulsion evaporation method and their release patterns were investigated in vitro. Various batches of microspheres with different size and drug content were obtained by changing the ratio of lorazepam to PLA, PLA concentration in the dispersed phase and stirring rate. Rod-like lorazepam crystals on microsphere surface, which were released rapidly and could act as a loading dose, were observed with increasing drug content. The release rate was increased with increase in drug contents and decrease in the molecular weight of PLA. The release rate of lorazepam for long-acting injectable delivery system in vitro, which would aid in Predicting in vivo release Profile, could be controlled by properly optimizing various factors affecting characteristics of microspheres.

• 한국세라믹학회지
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• 제52권6호
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• pp.531-534
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• 2015

In this work, we undertake a comparative study of the crystallographic microstructures and photo-catalytic properties of rutile $TiO_2$ nanorods grown on FTO facing up and down by a hydrothermal method. An analysis of the fine structures showed that $TiO_2$ nanorods grown on FTO facing up were mixed with sea urchin and microsphere. These structures induced a vertical orientation of the nanorods on FTO. The saturated photocurrent densities of the $TiO_2$ nanorods grown both up and down were $1.5mA/cm^2$ in the former case, the IPCE was increased to 10% at 300~350 nm. The onset potential (${\fallingdotseq}$ flat band potential) of the nanorods grown on FTO facing up is negatively shifted to a value of -0.31 V. This is caused by an increase in the surface state, in this case the number of oxygen vacancies, and by the formation of $Ti^{3+}$. Therefore, the FTO facing direction is considered as a critical factor during the hydrothermal reaction for $TiO_2$ growth so as to develop an efficient photo-catalytic system.

• 한국세라믹학회지
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• 제47권6호
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• pp.546-552
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• 2010

The achievement of high gas permeability is a key factor in the development of porous SiC ceramics for applications of hot gas filter, vacuum chuck, and air spindle. However, few reports on the gas permeability of porous SiC ceramics can be found in the literature. In this paper, porous SiC ceramics were fabricated at temperatures ranging from $1600^{\circ}C$ to $1800^{\circ}C$ using the mixing powders of SiC, silicon, carbon and boron as starting materials. In some samples, expanded hollow microspheres as a pore former were used to make a cellular pore structure. It was possible to produce Si bonded SiC ceramics with porosities ranging from 42% to 55%. The maximum bending strength was 58MPa for the carbon content of 0.2 wt% and sintering temperature of $1700^{\circ}C$. The increase of air permeability was accelerated by addition of hollow microsphere as a pore former.

• 대한의생명과학회지
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• 제12권4호
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• pp.443-450
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• 2006

To demonstrate their possibilities as an enhanced vaccine delivery system, protein-loaded Poly lactide glycolide copolymer (PLGA) microspheres were prepared with different physical characteristics. Ethyl acetate (EA) solvent extraction process was employed to prepare microspheres and the effects of process parameters on drug release properties were evaluated. The biodeuadability of microspheres was also evaluated by the pH change and GPC (Gel permeation chromatography). Primary IgG antibody responses in BALB/c mice were compared with protein saline solutions as negative controls and adsorbed alum suspensions as positive controls after single subcutaneous injection for in vivo studies. The microspheres showed a erosion with a highly porous structure and did not keep their spherical shape at 45 days and this result could be confirmed by GPC. In vitro release of proteinous drug showed initial burst effect in all batches of microspheres, followed by gradual release over the next 4 weeks. PLGA microspheres were degraded until 45 days and the secondary structure of OVA was not affected by the preparation method. Enzyme-linked immunosorbent assays demonstrated that the single subcutaneous administrations of OVA-loaded PLGA microspheres induced enhanced serum IgG antibody response in comparison to negative and positive controls. These results demonstrated that microspheres providing the controlled release of antigens might be useful in advanced vaccine formulations for the parenteral carrier system.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2002년도 제9차 국제심포지움 및 추계정기학술발표회
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• pp.52-52
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• 2002

Chitosan is a key compound of shrimp waste. It is a biopolymer, which is widely used in the field of medical Sciences. Chitosan-TPP (Tripolyphosphate) complex has more or less similar physical properties as Ca-alginate which can be used for the production of synthetic seeds. Possibility of the use of Chitosan-TPP complex as a matrix for encapsulation of somatic embryos was tested against the Ca-alginate complex (2.5w/v Na-alginate, 100mM CaCl2 at pH 5.5). Somatic embryos grown in the induction medium (IM) were drawn into the viscous chitosan solution (1%) and mixed well by inverting the tube carefully. Then the mixture was dropped at regular intervals into the tripolyphosphate (TPP) solution kept on a magnetic stirrer for bead formation. Synthetic seeds formed were washed and transferred into the incubation medium, then allowed either to air-dry or freeze-dry.(중략)

• Archives of Pharmacal Research
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• 제29권12호
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• pp.1179-1186
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• 2006

Cross-linked starch microspheres were prepared using different kinds of cross-linking agents. The influence of several parameters on morphology, size, swelling ratio and drug release rate from these microspheres were evaluated. These parameters included cross-linker type, concentration and the duration of cross-linking reaction. Microspheres cross-linked with glutaraldehyde had smooth surface compared with those prepared with epichlorhydrine or formaldehyde. The particle size increased with increasing the cross-linking time and increasing the drug loading. Swelling ratio of the particles was a function of cross-linker type but not the concentration or time of cross-linking. Drug release from starch microspheres was measured in phosphate buffer and also in phosphate buffer containing a-amylase. Results showed that microspheres cross-linked with epichlorhydrine released all their drug content in the first 30 minutes. However, cross-linking of the starch microspheres with glutaraldehyde or formaldehyde decreased drug release rate. SEM and drug release studies showed that cross-linked starch microspheres were susceptible to the enzymatic degradation under the influence of alpha-amylase. Changing the enzyme concentration from 5000 to 10,000 IU/L, increased drug release rate but higher concentration of enzyme (20,000 IU/L) caused no more acceleration.

• Archives of Pharmacal Research
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• 제28권9호
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• pp.1092-1096
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• 2005

Huperzine A-loaded microspheres composed of poly(D,L-lactide-co-glycolide) were prepared by an O/w emulsion solvent evaporation method. The characterization of the microspheres such as drug loading, size, shape and release profile was described. The in vitro release in the initial 7 days was nearly linear with $10\%$ released per day. Thereafter drug release rate became slow gradually and about $90\%$ drug released at day 21. The in vitro release rate determined by dialysis bag method had a good correlation with the in vivo release rate. Huperzine A aqueous solution was intramuscularly injected (i.m.) at 0.4mg/kg and microspheres were intra­muscularly injected at 8.4 mg eq huperzine A/kg in rats. The maxium plasma concentration $(C_{max})$ after i.m. microspheres was only $32\%$ of that after i.m. solution. Drug in plasma could be detectd until day 14 and about $5\%$ of administered dose was residued at the injection site at day 14. The relative bioavailability of huperzine A microspheres over a period of 14 days was $94.7\%$. Inhibition of acyecholinesterase activity (AchE) in rat's cortex, hippocampus and striatum could sustain for about 14 days. In conclusion, huperzine A-loaded microspheres possessed a prolonged and complete drug release with significant inhibition of AchE for 2 weeks in rats.

• 한국진공학회:학술대회논문집
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• 한국진공학회 2014년도 제46회 동계 정기학술대회 초록집
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• pp.283.1-283.1
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• 2014

최근 주위 환경에 존재하는 다양한 에너지를 전기에너지로 회수 또는 수확하는 에너지 하베스팅 기술(energy harvesting technology)이 크게 주목을 받고 있으며, 이와 더불어 압전 나노발전소자(piezoelectric nanogenerator)의 연구가 활발해 진행되고 있다. 한편, 수열합성법 또는 전기화학증착법을 이용하여 비교적 간단하게 수직으로 성장된 산화아연 나노로드(ZnO nanorod)는 광대역 에너지 밴드갭(wide bandgap energy)과 압전(piezoelectric)특성을 갖게 된다. 이렇게 수직 정렬된 나노로드의 기하학적 구조는 외부 물리적인 힘에 의해 구부러짐(bending) 변형이 일어나 압전특성이 효과적으로 일어나며, 이런 현상을 이용하여 압전 나노발전소자에 응용할 수 있다. 본 연구에서는 상부의 전극의 표면 거칠기(surface roughness)를 증가시켜 외부 힘에 의해 산화아연 나노로드가 효과적으로 변형을 일으켜 압전 특성을 향상시켰다. 실험을 위해, 산화아연 마이크로로드 어레이 (microrod arrays)와 실리카 마이크로스피어(silica microsphere)를 각각 템플릿으로 이용하여 그 위에 금(Au)를 증착하여 상부전극을 제작하였다. 산화아연 나노로드와 마이크로로드는 전기화학증착법을 이용해서 저온공정($75^{\circ}C$)으로 ITO가 코팅된 PET 기판위에 성장하였으며, 인가된 전압의 세기를 변화시켜 산하아연 구조물의 크기를 조절하였다. 또한 화합합성법으로 실리카 마이크로 스피어를 준비하였다. 이러게 제작된 상부전극을 통해 기존의 사용되었던 전극과 비교하여 성능이 향상됨을 확인하였으며, 이와 함께 이론적인 분석을 진행하였다.

• 농약과학회지
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• 제8권4호
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• pp.319-324
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• 2004

실리카 중공 미세구를 이용하여 방출 조절형 입제 농약을 제조합에 있어 실리카 중공 미세구 제조시 핵 제거 방법으로 열분해법을 사용하면 benfuracarb를 실리카 중공 미세구 중량의 2.67배까지 함침이 가능하였다. 이렇게 제조된 방출 조절형 입제 농약을 수중 방출 실험한 결과, 점결제로 ESO를 사용하였을 때 일정한 benfuracarb 방출 속도를 유지하여 10일부터 용액 중의 benfuracarb의 농도를 1.65 ppm 정도를 30일까지 유지되었다.