Mesostructure Evolution during Storage of Rubber Films from Washed Cream Latex and Skim Latex

2013 ◽  
Vol 844 ◽  
pp. 417-420
Author(s):  
Chalao Thepchalerm ◽  
Suwaluk Wisunthorn ◽  
Laurent Vaysse ◽  
Suda Kiatkamjornwong ◽  
Charoen Nakason ◽  
...  

Fresh field latex (FL) of Hevea brasiliensis was centrifuged to separate the major compartments: (i) the cream, (ii) the skim plus the C-serum, and (iii) the bottom fraction. Cream was dispersed in distilled water to prepare cream washed latex or CL sample. Skim was collected together with C-serum to prepare the skim latex or SKL sample. Then, films were made from FL, CL and SKL. The mesostructure (macromolecular structure and aggregates or gel) of the natural rubber films was studied by size exclusion chromatography coupled to a multiangular light scattering detector (SEC-MALS). The mesostructure was analyzed on fresh films and on films stored in the laboratory for three months (slow structuring). This study showed that FL and CL films had bimodal elution profiles of long and short polyisoprene chains as revealed by the two peaks on the chromatograms at low and high elution volumes, respectively. On the contrary, SKL films exhibited unimodal elution profiles at low elution volume and a highly abnormal molar masses elution profiles. After 3 months storage, the mesostructure of FL evolved dramatically especially the number-average molar masses (Mn), which increased by 60%. The mesostructure of CL films evolved at a lesser extent and, the mesostructure of SKL films exhibited no significant change. These results indicated (i) the skim rubber particles are not prone to slow structuring during storage in presence of serum and (ii) some constituents either in the serum or/and in the bottom fraction could still be present with cream and be involved in the slow structuring of cream particles latex.

2008 ◽  
Vol 1213 (2) ◽  
pp. 181-188 ◽  
Author(s):  
Chandy Kim ◽  
Marie-Hélène Morel ◽  
Jérôme Sainte Beuve ◽  
Stéphane Guilbert ◽  
André Collet ◽  
...  

2017 ◽  
Vol 90 (3) ◽  
pp. 445-454 ◽  
Author(s):  
Sébastien Rolere ◽  
Florian Deme ◽  
Jérôme Sainte-Beuve ◽  
Frédéric Bonfils

ABSTRACT Mechanical or thermal mastication experiments were performed on three commercial natural rubber (NR) samples of TSR10 grade made from latex of three different clones (GT1, PB235, and RRIM600). The mesostructure (different gel or aggregate fractions, structure of random coils of cis-1,4-polyisoprene) of all the NR samples was fully characterized by size exclusion chromatography coupled with multiangle light scattering (SEC-MALS), using pretreated SEC columns. This method was used to quantify and investigate the structure of the little-studied smaller microaggregates, constituting the microgel fraction smaller than 1 μm (Microgel<1μ) of NR. The three unmasticated NR samples showed no difference in terms of microaggregate structure. Conversely, microaggregates appeared denser after mastication. This phenomenon was found to depend on the mastication conditions, as mechanically masticated NR samples had smaller (lower radius of gyration) and more compact microaggregates than thermally masticated samples. Macrogel also behaved differently depending on the mastication conditions. Mechanical mastication conditions allowed a higher degradation of the macrogel compared with thermal mastication conditions.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Nicole L. McIntosh ◽  
Geoffrey Y. Berguig ◽  
Omair A. Karim ◽  
Christa L. Cortesio ◽  
Rolando De Angelis ◽  
...  

AbstractAdeno associated virus (AAV) capsids are a leading modality for in vivo gene delivery. Complete and precise characterization of capsid particles, including capsid and vector genome concentration, is necessary to safely and efficaciously dose patients. Size exclusion chromatography (SEC) coupled to multiangle light scattering (MALS) offers a straightforward approach to comprehensively characterize AAV capsids. The current study demonstrates that this method provides detailed AAV characterization information, including but not limited to aggregation profile, size-distribution, capsid content, capsid molar mass, encapsidated DNA molar mass, and total capsid and vector genome titer. Currently, multiple techniques are required to generate this information, with varying accuracy and precision. In the current study, a new series of equations for SEC-MALS are used in tandem with intrinsic properties of the capsids and encapsidated DNA to quantify multiple physical AAV attributes in one 20-min run with minimal sample manipulation, high accuracy, and high precision. These novel applications designate this well-established method as a powerful tool for product development and process analytics in future gene therapy programs.


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