Evaluation of two statistical methods for optimizing the feeding composition in anaerobic co-digestion: Mixture design and central composite design

2013 ◽  
Vol 131 ◽  
pp. 172-178 ◽  
Author(s):  
Xiaojiao Wang ◽  
Gaihe Yang ◽  
Fang Li ◽  
Yongzhong Feng ◽  
Guangxin Ren ◽  
...  
2021 ◽  
Author(s):  
Eugene Marfo Obeng ◽  
Clarence M. Ongkudon

Abstract The derivation of reduced sugars from lignocellulosic biomass requires an optimum blend of cellulolytic enzymes and reaction conditions that favour high sugar yield. In this respect, statistical design of experiment strategies become useful, but the technique is often misguided such that enzyme redundancy becomes overlooked. Herein, we demonstrate a systematic approach that involves simplex lattice mixture design and central composite design for optimizing enzyme cocktails for the saccharification of lignocellulosic biomass. The simplex lattice mixture design yielded 0.3333: 0.3333: 0.3333 of Celluclast (5%), Hemicellulase (5%) and Laccase (2%), respectively, as the optimum enzyme blend (volume) ratio for the saccharification of hydrothermally pretreated empty palm fruit bunch (EPFB, 10% solid loading). A subsequent application of central composite design resulted in 40 oC, pH 6 and 24 hrs as the optimum saccharification conditions. The individual Celluclast (5%) and Hemicellulase (5%) yielded a reduced sugar equivalence (RSE) of 1.77 mg/mL and 1.67 mg/mL, respectively. However, the blended enzyme cocktail upon subjection to simplex lattice mixture design and subsequent central composite design yielded an RSE of 2.215 mg/mL and 2.431 mg/mL, respectively. The overall results exemplify the significance of enzyme synergism in lignocellulosic biomass saccharification. The approach herein is intended as an easy-to-copy plan for optimizing enzyme cocktails.


2009 ◽  
Vol 00 (00) ◽  
pp. 090721051030036-8
Author(s):  
Jaleh Varshosaz ◽  
Solmaz Ghaffari ◽  
Mohammad Reza Khoshayand ◽  
Fatemeh Atyabi ◽  
Shirzad Azarmi ◽  
...  

Author(s):  
Bhikshapathi D. V. R. N. ◽  
Srinivas I

Repaglinide is a pharmaceutical drug used for the treatment of type II diabetes mellitus, it is characterized with poor solubility which limits its absorption and dissolution rate and delays onset of action. In the present study, immediate release solid dispersion of repaglinide was formulated by solvent evaporation technique. Repaglinide solid dispersions were prepared using PEG 8000, Pluronic F 127 and Gelucire 44/14 by solvent evaporation method. A 3-factor, 3-level central composite design employed to study the effect of each independent variable on dependent variables. FTIR studies revealed that no drug excipient interaction takes place. From powder X-ray diffraction (p-XRD) and by scanning electron microscopy (SEM) studies it was evident that polymorphic form of repaglinide has been converted into an amorphous form from crystalline within the solid dispersion formulation. The correlation coefficient showed that the release profile followed Higuchi model anomalous behavior and hence release mechanism was indicative of diffusion. The obtained results suggested that developed solid dispersion by solvent evaporation method might be an efficacious approach for enhancing the solubility and dissolution rate of repaglinide.


2012 ◽  
Vol 2 (4) ◽  
pp. 281-289
Author(s):  
Rattan Lal ◽  
Rakesh Kumar Marwaha ◽  
Deepti Pandita ◽  
Harish Dureja

Author(s):  
S. Abdullah ◽  
K.S.A. Latif ◽  
M.B. Besar ◽  
N.A.M. Zu ◽  
N. Hashim ◽  
...  

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