• Journal of Pharmaceutical Investigation
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• 제33권1호
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• pp.45-49
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• 2003

The solubility and stability of ondansetron hydrochloride (OS) in various vehicles were determined. The effect of cyclodextrins (CD) on the solubility of OS in water was determined by equilibrium solubility method. The solubility of OS at $32^{\circ}C$ increased in the rank order of isopropyl myristate (IPM) < propylene glycol laurate (PGL) ${\ll}$ propylene glycol monolaurate < propylene glycol monocaprylate (PGMC) < poly(ethylene glycol) 400 < diethylene glycol mono ethyl ether (DGME) < ethanol < poly(ethylene glycol) 300 < water (36.1 mg/ml) ${\ll}$ propylene glycol (PG) (283 mg/ml). The addition of PG or DGME to non-aqueous vehicles such as IPM, PGL and PGMC markedly increased the solubility of OS. The addition of CDs in water increased the solubility. Apparent stability constant for the CD complexation with OS was calculated to be $25.5\;M^{-1}$ for $2-hydroxypropyl-{\beta}-CD\;(2HP{\beta}CD)$. Twenty mM ${\beta}-CD$, 69.4 mM sulfobutyl ether ${\beta}-CD$ and 115.4 mM $2HP{\beta}CD$ increased the aqueous solubilty of OS 1.27, 2.18 and 1.85 times, respectively. OS was stable in buffered aqueous solution (pH 5.0). However, OS was relatively unstable in non-aqueous vehicles in the order of PG

• Journal of Microbiology and Biotechnology
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• 제15권4호
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• pp.855-858
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• 2005

The bioavailability of Ca is currently one of the most important topics in nutrition research and is correlated with gastrointestinal solubility. Thus, to increase the solubility of calcium, this study was undertaken to examine the effect of $\gamma$-PGA on intestinal Ca solubility. The calcium solubility increased when the amount of $\gamma$-PGA was increased, due to the inhibition of the formation of an insoluble Ca complex with phosphate. Therefore, when $\gamma$-PGA-500 (avg. MW 5,000 kDa) was added at 0.5 mg/ml, $75\%$ of the total Ca was soluble. The amount of soluble Ca uptake in the small intestine was investigated using Balb/c mice as an animal model system. The soluble Ca uptake in the mice orally administered with $\gamma$-PGA-500 (avg. MW 5,000 kDa) was significantly higher than that in the $\gamma$-PGA-l00 (avg. MW 1,000 kDa)-administered mice (P<0.05). Accordingly, these results strongly support the notion that the molecular size of $\gamma$-PGA is correlated with Ca solubility. The effects of other factors, such as casein phosphopeptide and vitamin D, on intestinal Ca absorption have also previously been investigated. Therefore, it is hoped that the present observations will help clarify the role of $\gamma$-PGA in Ca solubility and its industrial application as an additive.

• 한국자원식물학회지
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• 제11권3호
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• pp.272-278
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• 1998

This study was carried out to investigate the functional properties such as nitrogen solubility, emulsifying property , foaming capapcity , water and oil absorption of Camellia (Camellia japonica .) seed protein isolate in condition of distilled water and 0.5M NaCl solution at pH 2.0∼10.0. Nitrogen solubility of Camellia protein isolate in distilled water showed the minimum value at pH 4.0 and increased at pH lower or higher than the isoelectric point(pH 4.0). It was 90.0 %at pH 10.0 Nitrogen solubility of 0.5M NaCl solution showed a similar pattern with that of distrille dwater but was higher than that of distilled water except pH 2.0 and pH 10.0. Emulsifying activity of Camellia seed protein islate showed the minimum value at pH 4.0, but was higher at ether value of pH. Emulsifying stability of protein isolate was stable by heat treatment for 30min, at 80℃ and increased in 0.5M NaCl solution more than that of distille dwater. Foaming capacity of Camellia seed protein isolate in distill3ed water showed the minimum value near the isoelectric point, While it changed little at other values of pH. Foaming stability slowly decreased as, but didn't make a significant difference as time was delayed . Oil absorption was 1.4ml per a sample of 1g and water absorption was 0.9ml per a sample of 1g. The former was higher than the latter . The content of total amino acid of Camellia protein isolate was 43.67% and the major total amino acid of Camellia protein isolate was 43.67% and the major total amino acid was in the order of glutamic acid , arginine, aspartic acid, and leucine.

• 한국식품과학회지
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• 제22권3호
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• pp.350-356
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• 1990

참깨와 들깨 단백질을 알칼리에서 추출시킨 후 참깨는 pH6.0, 들깨는 pH4.0에서 침전시켜 분리 단백질을 제조하여 그들의 기능성 즉, 용해도, 유화성, 기포성, 유지 및 수분 흡착력 등을 pH와 염농도를 달리하여 측정하였다. 단백질 용해도는 참깨 단백질이 pH6.0에서, 들깨와 대두 단백질은 pH4.0에서 가장 낮아 등전점을 보이었고, pH2.0과 pH8.0 이상에서는 크게 증가하였다. 0.1M NaCl 첨가시에는 참깨 단백질과 들깨 단백질의 경우 전 pH 범위에서 단백질 용해도가 증가하였다. 유화력은 각 시료 단백질의 등전점 부근에서 가장 낮았으며 0.1M NaCl 첨가시에는 모든 시료들의 유화력이 증가되었으나 0.5M NaCl 농도에서는 오히려 감소되는 경향이었다. 유화안정성은 유화력과 비슷한 크기로 나타나, $80^{\circ}C$에서 30분 가열에서도 이들 단백질이 열에 안정함을 보이었다. 기포 형성력은 참깨와 들깨 단백질이 대두 단백질에 비해 현저히 낮았으며, 0.1M NaCl과 0.5M NaCl 첨가시에는 모두 그 값이 증가되는 경향을 보이었다. 기포 안정성은 대두 단백질이 10분 이내에 크게 감소된 반면 참깨와 들깨 단백질은 30분까지 완만하게 감소하였다. 유지 흡착력은 들깨 단백질이 가장 높은 값을 보였고, 수분 흡착력은 시료간에 차이가 없었다.

• 구강회복응용과학지
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• 제35권2호
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• pp.81-89
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• 2019

목적: 이 연구의 목적은 RMGIC에 레진 표면 코팅제를 적용하였을 때 용해도와 불소 유리량 간의 상관관계를 알아보는 것이다. 연구 재료 및 방법: 불소 유리량과 용해도 측정을 위해 표면 코팅제를 도포하지 않은 Fuji II $LC^{(R)}$, $Filtek^{TM}$ Z350XT와 G coat $plus^{TM}$를 도포한 Fuji II $LC^{(R)}$, $Permaseal^{(R)}$를 도포한 Fuji II $LC^{(R)}$를 준비하고 불소 유리량과 용해도를 측정하였다. 결과: 일간 불소 유리량은 표면 코팅제 간의 차이는 유의하지 않았다. 불소 누적 유리량은 56일에 RMGIC를 사용한 군에서 유의한 차이를 보였다(P < 0.05). 용해도 측정에서 표면 코팅제를 도포하지 않은 RMGIC가 다른 세 군에 비하여 7일 째에서만 유의한 차이를 보였다(P < 0.05). 결론: 표면 코팅제는 RMCIG에서 초기 용매에 의한 물성 저하를 막아 수복재 내부에 불소를 보존하며 추후 수복재의 불소의 방출과 저장에 대한 영향 또한 감소한다.

• 한국잠사곤충학회지
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• 제31권2호
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• pp.121-126
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• 1989

1. 제사용수의 pH가 총탄산이 낮은 용수에서는 견층 Sericin 용해에 미치는 영향이 적었지만, 총탄산이 높은 용수에서는 견층 Sericin 용해에 미치는 영향이 컸다. 2. 총탄산이 낮은 용수에서는 견층처리전후의 pH변화가 컸지만 총탄산이 높은 용수에서는 그 변화가 적었다. 3. 무탄산 증류수로 표준경도용액을 만들어 견층을 처리한 결과 경도가 높고 낮은데 대한 Sericin 용액관계는 없었다.

• 한국수산과학회지
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• 제42권6호
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• pp.574-579
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• 2009

Acid- and pepsin-solubilized collagens were extracted from the skin of shark (Isurus oxyrinchus) and their physicochemical properties were characterized by amino acid analysis, SDS-PAGE, the composition of collagen types, solubility and denaturation temperature. Acid - and pepsin-solubilized collagens from shark skin had an imino acid of 188.8 and 186.2 residues/1,000 amino acids, respectively. SDS-PAGE showed two different${\alpha}$ chains ($\alpha1$ and $\alpha2$) and $\beta$-component. The component ratio of type I and V was 10:1, and the type III was not found. Solubility of acid-soluble collagen was low in the range of pH 6.0 to pH 11.0. On the other hand, pepsin-solubilized collagen showed a low solubility in the range of pH 7.0-9.0. Temperature for denaturation of acid- and pepsin-solubilized collagens were $25^{\circ}C$ and $27^{\circ}C$, respectively.

• KSBB Journal
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• 제31권4호
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• pp.219-227
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• 2016

Valsartan, a drug for the treatment of cardiovascular disease, exhibited low bioavailability which was caused by, at least in part, limited solubility at low pH. Present investigation deals with the preparation and characterization of gastro-retentive drug delivery system (GRDDS) using valsartan solid dispersion. We prepared solid dispersion using surfactants (Poloxamer 407) and alkalizer ($Na_2CO_3$) which may to be useful for improving solubility of valsartan at low pH and evaluated by saturated solubility of valsartan in distilled water. Valsartan gastro-retentive (GR) tablets containing solid dispersion prepared and evaluated by weight variation, floating time and dissolution rate. Compression at lower pressures resulted in the tablets floating over simulated gastric fluid (pH 1.2) for more than 17 h. In vitro release of valsartan from GR tablet was dependent on the amount of poloxamer 407 and hydroxypropyl methylcellulose. On the basis of evaluation parameter, formulation E-3 was selected as a final formulation. Therefore, it can be concluded that the GR tablets containing solid dispersion may be exploited successfully for the delivery of poorly drug such as valsartan.

• 대한소아치과학회지
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• 제49권4호
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• pp.379-391
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• 2022

이 연구는 premixed MTA 제재와 기존 치수복조제의 경화 전, 후의 pH 값 그리고 칼슘, 황, 스트론튬 이온의 유리량, 용해도를 비교했다. 사용된 재료는 다음과 같다 : 레진 강화형 칼슘실리케이트(TheraCal LC^®; TLC), 레진 강화형 수산화칼슘(UBP, Ultra-Blend^TM plus), 2종류의 premixed MTA(Endocem MTA^® premixed regular [EMPR] and Well-Root^TM PT [WRP]). 각 재료의 시편은 경화 전, 경화 후 2군으로 나누어 준비한 뒤 증류수에 보관하였다. pH, 용해도를 측정하였으며 ICP-AES를 이용한 칼슘, 황, 스트론튬의 3가지 이온 유리량을 측정하였다. 경화 후 군에서 TLC와 UBP의 pH 값은 감소했다. 그러나 premixed MTA 재료의 pH 값은 증가했다. TLC는 다른 재료와 비교하여 스트론튬 이온 유리량이 더 많았다. 동시에 EMPR에서 황이온 유리량이 높았다(p < 0.05). 경화 후 군에서 칼슘 이온 방출은 두 종류의 premixed MTA에서 더 높았다(p < 0.05). 경화 후 군에서 용해도는 Kruskal-Wallis 서 test를 이용하여 통계분석하였고 Mann-Whitney U test를 이용하여 사후검정하였다. 결론적으로 레진 강화형 칼슘 실리케이트 시멘트, 레진 강화형 수산화칼슘 시멘트, 2종류의 premixed MTAs 모두 경화 후 알칼리성 pH 값과 낮은 용해도를 가지고 있었으며 다양한 이온을 유리했다.

• Archives of Pharmacal Research
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• 제18권6호
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• pp.427-433
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• 1995

A microscopic mass balance approach has hsown that the initial saturation (Is), absorption number (An), dose number (Do), and dissolution number (Dn) are four fundamental dimensionless parameters that can be used to estimate the fraction dose absorbed (F)l of suspensions of poorly soluble drugs in humans. The dissolution number of a drug increases with decreasing its particle size. The effect of micronization on F for suspensions was investigated in terms of Dn. About 90% of maximal F can be achieved at $Dn{\approx}2$. Increasing the solubility of a drug results in better oral absorption through increasing Dn and decreasing the solubility of a drug results in better oral absorption through increasing Dn and decreasing Do. The fractions dose absorbed of digoxin, griseofulvin, and benoxaprofen agree with predicted F values sorbed by reducing particle size, while absorption of drugs with high Do and low Dn is limited by solubility and requires higher solubility to enhance the fraction dose absorbed in addition to micronization. Solubility at the physiological pH should be used for the estimation of the fraction dose absorbed.