scholarly journals Mass Transfer in a Geologic Environment

1984 ◽  
Vol 44 ◽  
Author(s):  
S. J. Zavoshy ◽  
P. L. Chambre' ◽  
T. H. Pigford
Keyword(s):  
Mass Transfer ◽  
Analytical Solution ◽  
Dissolution Rate ◽  
Surface Chemical Reaction ◽  
Porous Rock ◽  
Important Species ◽  
Rate Of Dissolution ◽  
Diffusive Mass Transfer ◽  
Dissolved Species ◽  
Surface Liquid

AbstractA new analytical solution is presented that predicts the rate of dissolution of species from a waste package surrounded by a wet porous medium. By equating the rate of diffusive mass transfer into the porous rock to the rate of liquid-surface chemical reaction, an analytical solution for the timedependent dissolution rate and the time-dependent concentration of dissolved species at the waste surface is obtained. From these results it is shown that for most of the important species in a package of radioactive waste the surface liquid quickly reaches near-saturation concentrations and the dissolution rate can be predicted by the simpler theory that assumes saturation concentrations in the surface liquid.

scholarly journals Transient and Steady-State Radionuclide Transport Through Penetrations in Nuclear Waste Containers

1986 ◽  
Vol 84 ◽  
Author(s):  
P. L. Chambre ◽  
W. W.-L. Lee ◽  
C. L. Kim ◽  
T. H. Pigford
Keyword(s):  
Mass Transfer ◽  
Steady State ◽  
Nuclear Waste ◽  
Porous Rock ◽  
Intimate Contact ◽  
Transfer Rates ◽  
Diffusive Mass Transfer ◽  
Solutions Of Equations ◽  
Multiple Holes ◽  
Significant Mass

AbstractIn this paper we analyze the transport of radionuclides through penetrations in nuclear waste containers. Penetrations may result from corrosion or cracks and may occur in the original container material, in degraded or corroded material, or in deposits of corrosion products. We do not consider how these penetrations occur or the characteristics of expected penetrations in waste containers. We are concerned only with the analytical formulation and solutions of equations to predict rates of mass transfer through penetrations of specified size and geometry. Expressions for the diffusive mass transfer rates through apertures are presented. We present numerical illustrations for steady-state mass-transfer rates through a circular hole, including concentration isopleths. The results are extended to multiple holes, including a criterion for hole spacing wherein superposition of single-hole solutions can be used. Results illustrated for holes in thin-walled containers show that significant mass transfer can occur even if a small fraction of the container area is perforated. We also illustrate the case of holes facing a water gap, instead of being in intimate contact with porous rock. In this case the radionuclide flux from many small holes approaches that from a bare waste cylinder.

Diffusive mass transfer in island films

1978 ◽  
Vol 125 (7) ◽  
pp. 489-525 ◽  
Author(s):  
Ya.E. Geguzin ◽  
Yu.S. Kaganovskii
Keyword(s):  
Mass Transfer ◽  
Diffusive Mass Transfer ◽  
Island Films

Formulation and Evaluation of Nanosuspension of Simvastatin

2015 ◽  
Vol 8 (2) ◽  
pp. 2858-2873
Author(s):  
Rupali L. Shid ◽  
Shashikant N. Dhole ◽  
Nilesh Kulkarni ◽  
Santosh L Shid
Keyword(s):  
Particle Size ◽  
Zeta Potential ◽  
Factorial Design ◽  
Dissolution Rate ◽  
In Vitro Dissolution ◽  
Total Drug ◽  
23 Factorial Design ◽  
Rate Of Dissolution

Poor water solubility and slow dissolution rate are issues for the majority of upcoming and existing biologically active compounds. Simvastatin is poorly water-soluble drug and its bioavailability is very low from its crystalline form. The purpose of this study wasto increase the solubility and dissolution rate of simvastatin by the  preparation of nanosuspension by emulsification solvent diffusion method at laboratory scale. Prepared nanosus-pension was evaluated for its particle size and in vitro dissolution study and characterized by zeta potential,differential scanning calorimetry (DSC) and X-Ray diffractometry (XRD), motic digital microscopy, entrapment efficiency, total drug content, saturated solubility study and in vivo study. A 23 factorial design was employed to study the effect of independent variables, amount of SLS (X1), amount of PVPK-30 (X2) and poloxamer-188 (X3) and dependent variables are total drug content and polydispersity Index. The obtained results showed that particle size (nm) and rate of dissolution has been improved when nanosuspension prepared with the higherconcentration of PVPK-30 with the higher concentration of PVP K-30 and Poloxamer-188 and lower concentration of SLS. The particle size and zeta potential of optimized formulation was found to be 258.3 nm and 23.43. The rate of dissolution of the optimized nanosuspension was enhanced (90% in 60min), relative to plain simvastatin  (21% in 60 min), mainly due to the formation of nanosized particles. These results indicate the suitability of 23 factorial  design for preparation of simvastatin loaded nano-suspension significantly improved in vitro dissolution rate and thus possibly enhance fast onset of therapeutic drug effect. In vivo study shows increase in bioavailability in nanosuspension formulation than the plain simvastatin drug.

Enhanced oral bioavailability of Etodolac by liquisolid compact technique: optimisation, in-vitro and in-vivo evaluation

2020 ◽  
Vol 17 ◽  
Author(s):  
Bhumin K. Pathak ◽  
Meenakshi Raghav ◽  
Arti R. Thakkar ◽  
Bhavin A. Vyas ◽  
Pranav J. Shah
Keyword(s):  
Dissolution Rate ◽  
Amorphous State ◽  
Immediate Release ◽  
Angle Of Repose ◽  
Oral Suspension ◽  
Load Factor ◽  
In Vivo Evaluation ◽  
Rate Of Dissolution ◽  
Q 30

Background: Poor dissolution of Etodolac is one of the major challenges in achieving the desired therapeutic effect in oral therapy. Objective: This study aimed to assess the potential of liquisolid compact technique in increasing the rate of dissolution of Etodolac and thus its bioavailability. Methods: Liquisolid compacts were prepared using PEG 400, Avicel PH-200 and Aerosil 200 as non-volatile liquid, carrier and coating material respectively. Optimisation was carried out by applying a 32 full factorial design using Design expert software 11.0.3.0 to examine the effects of independent variables (load factor and carrier: coating ratio) on dependent variables (angle of repose and % cumulative drug release at 30 min [Q 30 min]).Assessment of bioavailability was based on pharmacokinetic study in rabbits and pharmacodynamics evaluation in rats respectively. Results: The formulation M3 was identified as the optimised formulation based on the better flow (lower angle of repose) and a higher rate of dissolution (Q 30 min >95%). The higher dissolution rate could be due to conversion of Etodolac into an amorphous molecularly dispersed state, availability of larger surface area, enhancement of aqueous solubility and enhanced wetting of drug particles. Studies with DSC, XRD, and SEM verified the transformation of Etodolac from crystalline to amorphous state, a key factor responsible for improving the dissolution rate. Pharmacokinetic profile of M3 was prominent, demonstrating higher absorption of Etodolac in comparison of oral suspension and immediate-release conventional tablets in rabbits. Liquisolid formulation exhibited 27% increment in paw thickness as compared to 57% and 46% increments for oral suspension and immediate-release conventional tablets respectively, after 7 hrs in carrageenan-induced paw model in rats. Conclusion: The results indicated liquisolid compact technique to be a promising strategy to enhance the bioavailability of Etodolac.

Investigations of process parameters during dissolution studies of drug loaded 3D printed tablets

2021 ◽  
pp. 095441192199358
Author(s):  
Varun Sharma ◽  
Khaja Moinuddin Shaik ◽  
Archita Choudhury ◽  
Pramod Kumar ◽  
Prateek Kala ◽  
...  
Keyword(s):  
Dissolution Rate ◽  
Process Parameters ◽  
Empirical Relation ◽  
Three Dimensional ◽  
Critical Parameters ◽  
Fused Deposition Modelling ◽  
Fused Deposition ◽  
Rate Of Dissolution ◽  
3D Printed ◽  
Percentage Release

The present research paper attempts to study the effect of different process parameters on the dissolution rate during 3D printed tablets. Three-dimensional printing has the potential of serving tailored made tablets to cater personalized drug delivery systems. Fluorescein loaded PVA filaments through impregnation route was used to fabricate tablets based on Taguchi based design of experimentation using Fused Deposition Modelling (FDM). The effect of print speed, infill percentage and layer thickness were analyzed to study the effect on rate of dissolution. Infill percentage followed by print speed were found to be critical parameters affecting dissolution rate. The data analysis provided an insight into the study of interaction among different 3D printing parameters to develop an empirical relation for percentage release of the drug in human body.

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