Simulation study of monoclonal antibody production using superpro, upstream process / (Record no. 1708)

MARC details
000 -LEADER
fixed length control field 02446nam a2200241 a 4500
001 - CONTROL NUMBER
control field vtls000045140
003 - CONTROL NUMBER IDENTIFIER
control field KUKTEM
005 - DATE AND TIME OF LATEST TRANSACTION
control field 20251114204422.0
008 - FIXED-LENGTH DATA ELEMENTS--GENERAL INFORMATION
fixed length control field 100219t2009 my ao f m 000 0 eng d
020 ## - INTERNATIONAL STANDARD BOOK NUMBER
International Standard Book Number THE0002290(Local)
039 #9 - LEVEL OF BIBLIOGRAPHIC CONTROL AND CODING DETAIL [OBSOLETE]
Level of rules in bibliographic description 201905241223
Level of effort used to assign nonsubject heading access points shamsul
Level of effort used to assign subject headings 201108030917
Level of effort used to assign classification Fida
Level of effort used to assign subject headings 201107132307
Level of effort used to assign classification VLOAD
-- 201002191023
-- kam
040 ## - CATALOGING SOURCE
Original cataloging agency UMP
090 ## - LOCALLY ASSIGNED LC-TYPE CALL NUMBER (OCLC); LOCAL CALL NUMBER (RLIN)
Classification number (OCLC) (R) ; Classification number, CALL (RLIN) (NR) QR186.85 .S53 2009 rs Bc.
100 0# - MAIN ENTRY--PERSONAL NAME
Personal name Mohd Shamsul Husin
245 10 - TITLE STATEMENT
Title Simulation study of monoclonal antibody production using superpro, upstream process /
Statement of responsibility, etc. Mohd Shamsul Bin Husin
246 3# - VARYING FORM OF TITLE
Title proper/short title Simulation study of monoclonal antibody production using superpro, upstream process
Medium [computer file]
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Place of publication, distribution, etc. Kuantan : UMP, 2009
300 ## - PHYSICAL DESCRIPTION
Extent 30 p. :
Other physical details ill. (some col.) ;
Dimensions 30 cm. +
Accompanying material 1 computer disc
502 ## - DISSERTATION NOTE
Dissertation note Project paper (Bachelor of Chemical Engineering (Biotechnology)) -- Universiti Malaysia Pahang – 2009
520 3# - SUMMARY, ETC.
Summary, etc. The purpose of this study is to approximate hybridoma growth kinetic model by comparing simulation result from SuperPro Designer® and experimental result. Modeling of hybridoma include calculation of mass for 1 cell and its density. Two kinetic models tested in this study; experimental correlation and de Tremblay et al. (1992). Simplification need to be made as this will allow selected model to be used in SPD. Value of μmax, KsGLN, KsGLC are 1.09 d-1 (0.05 h-1), 0.3 mM (43.85 mg/L) and 0.1 mM (18.02 mg/L) respectively for de Tremblay and for experimental correlation, their values are 0.158 h-1, 0.0016 mM (0.23 mg/L) and 12.05 mM (2170.93 mg/L) respectively. Experimental data shows no stationary phase but simulation results show stationary phase. From simulation, cell count of 195907.7 while final concentration of glucose, glutamine, ammonia and lactate are 16.38, 4.07, 3.01 and 5.59 mmol/L respectively (experimental correlation) and cell count of 196185.73 while final concentration of glucose, glutamine, ammonia and lactate are 10.73, 2.09, 6.07 and 11.30 mmol/L respectively (de Tremblay). Serious deviations occurred because of simplification on de Tremblay model and inaccurate prediction of glutamine effect on hybridoma’s growth. Metabolic reaction used without taking hybridoma real behavior into account. Simulation shows exponential phase without having going through lag phase.
650 #0 - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element Monoclonal antibodies
Holdings
Withdrawn status Lost status Damaged status Not for loan Home library Current library Date acquired Total checkouts Full call number Barcode Date last seen Copy number Price effective from Koha item type
  Not lost   Not for loan UMPLIB GAMBANG UMPLIB GAMBANG 04/09/2019   QR186.85 .S53 2009 rs Bc. 0000042961 04/09/2019 1 04/09/2019 Final Year Report
  Not lost   Not for loan UMPLIB GAMBANG UMPLIB GAMBANG 04/09/2019   CD 4012 | QR186.85 .S53 2009 rs Bc. 0000042962 04/09/2019 1 04/09/2019 Final Year Report

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