• Title/Summary/Keyword: T-A formulation

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Characterization of Physicochemical Properties of Ferulic Acid

  • Sohn, Young-Taek;Oh, Jin-Hee
    • Archives of Pharmacal Research
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    • v.26 no.12
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    • pp.1002-1008
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    • 2003
  • Ferulic acid (3-methoxy, 4-hydroxy cinnamic acid) is a flavoid component possessing antioxidant property. The compound is currently under development as a new drug candidate for the treatment of the dementia. The objective of this preformulation study was to determine the physicochemical properties of ferulic acid. The n-octanol to water partition coefficients of ferulic acid were 0.375 and 0.489 at the pHs of 3 and 10, respectively. Accelerated stability study for ferulic acid indicated that the t 90 value for the drug was estimated to be 459 days at $25^{\circ}C$. Ferulic acid was also found to be unstable under the relative humidity of more than 76%, probably because of the hygroscopic nature of the drug. In order to study compatibility of ferulic acid with typical excipients, potential change in differential scanning calorimetry spectrum was studied in 1: 1 binary mixtures of ferulic acid and typical pharmaceutical excipients (e.g., Aerosil, Avicel, CMC, Eudragit, lactose, PEG, PVP, starch and talc). Avicel, CMC, PVP and starch were found to be incompatible with ferulic acid, indicating the addition of these excipients may complicate the manufacturing of the formulation for the drug. Particle size distribution of ferulic acid powder was in the size range of 10-190 $\mu$m with the mean particle size of 61 $\mu$m. The flowability of ferulic acid was apparently inadequate, indicating the granulation may be necessary for the processing of the drug to solid dosage forms. Two polymorphic forms were obtained by recrystallization from various solvents used in formulation. New polymorphic form of ferulic acid, Form II, was obtained by recrystallization from 1,4-dioxane. The equilibrium solubility for Form I was approximately twice of that for Form II. The dissolution rate of Form II was higher than that of Form I in the early phase (<6 min). Therefore, these physicochemical information has to be taken in the consideration for the formulation of ferulic acid.

Development of Clotrimazole Gels for Enhanced Transdermal Delivery

  • Cho, Hwa-Young;Kim, Dal-Keun;Park, ung-Chan;Kang, Chung;Oh, In-Joon;Kim, Seong-Jin;Shin, Sang-Chu
    • Journal of Pharmaceutical Investigation
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    • v.39 no.6
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    • pp.437-443
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    • 2009
  • To develop a topical bioadhesive formulation of clotrimazole for enhanced transdermal delivery, hydroxypropyl methylcellulose gel containing permeation enhancer was formulated and permeation studies were carried out. The release characteristics of the drug from the gel formulation were examined according to the receptor medium, drug concentration, and temperature. The rate of drug release from the gel increased with increasing drug concentration and temperature. The activation energy (Ea) of drug permeation, which was calculated from the slope of log P versus 1/T plots, was 14.41kcal/mol for a 1%(w/w) loading dose. The enhancer, such as saturated, unsaturated fatty acids, pyrrolidones, propylene glycol derivatives, glycerides, and non-ionic surfactants, were incorporated onto the gels to increase the amount of drug permeation into the skin. Among the enhancers used, polyoxyethylene 2-oleyl ether showed the highest level of enhancement. These results show that clotrimazole gels containing polyoxyethylene 2-oleyl ether could be used for the enhanced transdermal delivery of clotrimazole.

Sensitivity Analysis for Flexural Behaviors of PSC Members (프리스트레스트 콘크리트 휨 부재의 민감도 해석)

  • Lee, Jon-Ja;Lee, Bong-Goo;Kim, Min-Joo;Lee, Yong-Hak
    • Journal of the Korea institute for structural maintenance and inspection
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    • v.6 no.2
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    • pp.183-194
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    • 2002
  • A general procedure to evaluate the sensitivity of design variables to stresses and strains in PSC flexural members is proposed. To accomplish the purpose of this study, long-term losses including creep, shrinkage, and PS steel relaxation are formulated based on the equilibrium states of the deformed sectional geometry. Thereby, the formulation follows the basic steps which consider the fundamental formulas adopted by CEB-FIP, ACI, and KCI rather than the age adjusted effective modulus concept. Twenty-one design variable including the material and geometrical properties of concrete, nonprestressing steel and prestressing steel, and the geometry of the cross section are considered in the sensitivity analysis. The gradients of the stresses and strains needed for the sensitivity assessment are calculated in a closed format. The derived formulation is applied to the T-type section PSC beam with prestressing and nonprestressing steels for the sensitivity analysis. The analytically calculated sensitivity results are compared with those numerically calculated to ensure the validity of the proposed procedure.

A User Equilibrium Transit Assignment Model with Vehicle Capacity Constraint (차량용량을 고려한 대중교통 통행배정모형구축에 관한 연구)

  • 이성모;유경상;전경수
    • Journal of Korean Society of Transportation
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    • v.14 no.3
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    • pp.27-44
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    • 1996
  • The purpose of the thesis is providing a new formulation for the transit assignment problem. The existing models dealing with the transit assignment problem don't consider the congestion effects due to the insufficient capacity of transit vehicles. Besides, these models don't provide solutions satisfying the Wardrop's user equilibrium conditions. The congestion effects are considered to be concentrated at the transit stops. For the transit lines, the waiting times at the transit stops are dependent on the passenger flows. The new model suggests the route section cost function analogous to the link performance function of the auto assignment to reflect the congestion effects in congested transit network. With the asymmetric cost function, the variational inequality programming is used to obtain the solutions satisfying Wardrop's condition. The diagonalization algorithm is introduced to solve this model. Finally, the results are compared with those of EMME/2.

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Stability conditions for Time-delayed LPV systems (시간 지연 선형 파라메타 변형 시스템의 안정화 조건에 관한 연구)

  • Jeong, Chang-Ki;Kang, Byung-Hoon;Ko, Jeong-Wan;Park, Poo-Gyeon
    • Proceedings of the KIEE Conference
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    • 2007.10a
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    • pp.55-56
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    • 2007
  • In this paper, a delay-dependent stability criterion for time-delayed linear parameter varying (LPV) systems is considered. Stability criterion has been developed on the basis of including x(t-h) and x(t) and introducing free variables to eliminate model dynamics. Since the resultant criterion is formed parameterized linear matrix inequalities (PLMIs), we propose a relaxation technique that allows to find an LMI formulation. Examples demonstrate the efficiency of the criterion over the existing results.

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Adaptive Video Streaming over HTTP with Dynamic Resource Estimation

  • Thang, Truong Cong;Le, Hung T.;Nguyen, Hoc X.;Pham, Anh T.;Kang, Jung Won;Ro, Yong Man
    • Journal of Communications and Networks
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    • v.15 no.6
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    • pp.635-644
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    • 2013
  • Adaptive hypertext transfer protocol (HTTP) streaming has become a new trend to support adaptivity in video delivery. An HTTP streaming client needs to estimate exactly resource availability and resource demand. In this paper, we focus on the most important resource which is bandwidth. A new and general formulation for throughput estimation is presented taking into account previous values of instant throughput and round trip time. Besides, we introduce for the first time the use of bitrate estimation in HTTP streaming. The experiments show that our approach can effectively cope with drastic changes in connection throughput and video bitrate.

Preparation of Lacosamide Sustained-release Tablets and Their Pharmacokinetics in Beagles and Mini-pigs

  • Ahn, Jae Soon;Kim, Kang Min;Nam, Dae Sik;Kang, Kyoung Un;Choi, Peter S.;Jeong, Seo Young
    • Bulletin of the Korean Chemical Society
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    • v.35 no.2
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    • pp.557-561
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    • 2014
  • The aim of the present study was to improve dosing of lacosamide, a functionalized amino acid used as an antiepileptic agent, from twice daily to once daily for the convenience of patients. A sustained-release lacosamide tablet was developed and dissolution testing was employed to determine in vitro release behavior using water or buffer solutions at pH 1.2, 4.0, or 6.8. Lacosamide was released for 12 h from the sustainedrelease (SR) tablet, as compared to complete release within 1 h from an immediate-release $Vimpat^{(R)}$ tablet. Each formulation (100 mg) was orally administered to six beagle dogs and six mini-pigs under fasted conditions, and pharmacokinetic parameters such as the area under the concentration time curve ($AUC_t$), the maximum plasma concentration ($C_{max}$), and the time at which this occurred ($T_{max}$) were calculated. These results showed similar values for $AUC_t$, $C_{max}$, and $T_{max}$ following oral administration of immediate-release ($Vimpat^{(R)}$) and SR lacosamide tablets.

Endophytic Trichoderma citrinoviride isolated from mountain-cultivated ginseng (Panax ginseng) has great potential as a biocontrol agent against ginseng pathogens

  • Park, Young-Hwan;Mishra, Ratnesh Chandra;Yoon, Sunkyung;Kim, Hoki;Park, Changho;Seo, Sang-Tae;Bae, Hanhong
    • Journal of Ginseng Research
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    • v.43 no.3
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    • pp.408-420
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    • 2019
  • Background: Ginseng (Panax ginseng Meyer) is an invaluable medicinal plant containing various bioactive metabolites (e.g., ginsenosides). Owing to its long cultivation period, ginseng is vulnerable to various biotic constraints. Biological control using endophytes is an important alternative to chemical control. Methods: In this study, endophytic Trichoderma citrinoviride PG87, isolated from mountain-cultivated ginseng, was evaluated for biocontrol activity against six major ginseng pathogens. T. citrinoviride exhibited antagonistic activity with mycoparasitism against all ginseng pathogens, with high endo-1,4-${\beta}$-D-glucanase activity. Results: T. citrinoviride inoculation significantly reduced the disease symptoms caused by Botrytis cinerea and Cylindrocarpon destructans and induced ginsenoside biosynthesis in ginseng plants. T. citrinoviride was formulated as dustable powder and granules. The formulated agents also exhibited significant biocontrol activity and induced ginsenosides production in the controlled environment and mountain area. Conclusion: Our results revealed that T. citrinoviride has great potential as a biological control agent and elicitor of ginsenoside production.

A new bridge-vehicle system part II: Parametric study

  • Chan, Tommy H.T.;Yu, Ling;Yung, T.H.;Chan, Jeffrey H.F.
    • Structural Engineering and Mechanics
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    • v.15 no.1
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    • pp.21-38
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    • 2003
  • The formulation of a new bridge-vehicle system using shell with eccentric beam elements has been introduced in a companion paper (Part I). The new system takes into account of the contribution of the twisting and pitching modes of vehicles to the bridge responses. It can also be used to study the dynamic transverse load distribution of a bridge. This paper presents a parametric study on the impact induced by one vehicle or multi-vehicle running across a bridge using the proposed model. Several parameters were considered as variables including the mass ratio, the speed parameter, the frequency ratio and the axle spacing parameter to investigate their effects on the impact factor. A total number of 189 cases were carried out in this parametric study. Within the realistic range of vehicle considered, the maximum impact factors could be 2.24, 1.78 and 1.49 for bridges with spans 10 m, 20 m and 30 m respectively.

Effects of Fiber-rich Apple and Apricot Powders on Cookie Quality

  • Seker, Ibrahim T.;Ozboy-Ozbas, Ozen;Gokbulut, Incilay;Ozturk, Serpil;Koksel, Hamit
    • Food Science and Biotechnology
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    • v.18 no.4
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    • pp.948-953
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    • 2009
  • Apple and apricot powders (APL-P and APR-P) were produced from apple and apricot fruits and they were used in cookie formulation at the levels of 10-40% (in flour bases). The APL-P and APR-P were rich in terms of total dietary fiber (TDF) and antioxidant power. The APR-P supplemented cookies had higher spread ratio and lower hardness values than the APL-P supplemented ones at all addition levels. The color values of the APR-P supplemented cookies were all acceptable. Overall sensory scores of the cookies supplemented with APL-P and APR-P were not significantly different from the control up to 20% addition. TDF contents of the supplemented cookies increased significantly with increasing addition level (p<0.01). The replacement of flour by APL-P and APR-P in wire-cut cookies showed that the physical characteristics and textural properties of the cookies were significantly affected (p<0.01) and APR-P appeared to be a more suitable replacer of flour than APL-P. Addition of both fruit powders upto 20% into the cookie formulation were evaluated as acceptable in terms of the sensory properties.