Methods for identification, quantification and characterization of polyhydroxyalkanoates

2016 ◽  
Vol 5 (04) ◽  
pp. 4977 ◽  
Author(s):  
Suchitra Godbole

Polyhydroxyalkanoates (PHAs) are the polymers of hydroxyalkanoates that accumulate as a carbon/energy storage material in various microorganisms. PHAs have been attracting considerable attention as biodegradable substitutes for conventional polymers, because of their similar material properties to conventional plastics. A number of review articles on the general features of PHAs, the physiology, genetics and molecular biology, the development of PHAs having novel monomer constituents, production processes, biodegradation of PHAs are available. Recently much effort has been devoted to develop a process for the economical production of PHAs. The isolation, analysis and characterization of PHAs are important factors for any process development. A number of methods have been developed for the analysis of PHAs. This paper is an effort to compile the methods available for the identification, quantitative estimation and characterization of PHAs. The methods described in this paper include- staining reactions, spectrophotometric methods, infrared and FTIR spectroscopy, HPLC, gas chromatography and GC-MS analysis, NMR spectroscopy, flow cytometry and spectrofluorometry, molecular weight determination and thermal analysis. The methods have been discussed with their advantages and disadvantages. Recent developments in the analysis of PHAs have also been discussed.

Energy ◽  
2015 ◽  
Vol 89 ◽  
pp. 601-609 ◽  
Author(s):  
Iñigo Ortega-Fernández ◽  
Nicolas Calvet ◽  
Antoni Gil ◽  
Javier Rodríguez-Aseguinolaza ◽  
Abdessamad Faik ◽  
...  

2019 ◽  
Vol 317 ◽  
pp. 746-752 ◽  
Author(s):  
Milica M. Gvozdenović ◽  
Braninir Z. Jugović ◽  
Bojan M. Jokić ◽  
Enis S. Džunuzović ◽  
Braninimir N. Grgur

2021 ◽  
Vol 33 ◽  
pp. 102159
Author(s):  
B. Chen ◽  
K. Johannes ◽  
M. Horgnies ◽  
V. Morin ◽  
F. Kuznik

Author(s):  
H. Sur ◽  
S. Bothra ◽  
Y. Strunk ◽  
J. Hahn

Abstract An investigation into metallization/interconnect failures during the process development phase of an advanced 0.35μm CMOS ASIC process is presented. The corresponding electrical failure signature was electrical shorting on SRAM test arrays and subsequently functional/Iddq failures on product-like test vehicles. Advanced wafer-level failure analysis techniques and equipment were used to isolate and identify the leakage source as shorting of metal lines due to tungsten (W) residue which was originating from unfilled vias. Further cross-section analysis revealed that the failing vias were all exposed to the intermetal dielectric spin-on glass (SOG) material used for filling the narrow spaces between metal lines. The outgassing of the SOG in the exposed regions of the via prior to and during the tungsten plug deposition is believed to be the cause of the unfilled vias. This analysis facilitated further process development in eliminating the failure mechanism and since then no failures of this nature have been observed. The process integration approach used to eliminate the failure is discussed.


2001 ◽  
Vol 66 (9) ◽  
pp. 1315-1340 ◽  
Author(s):  
Vladimir J. Balcar ◽  
Akiko Takamoto ◽  
Yukio Yoneda

The review highlights the landmark studies leading from the discovery and initial characterization of the Na+-dependent "high affinity" uptake in the mammalian brain to the cloning of individual transporters and the subsequent expansion of the field into the realm of molecular biology. When the data and hypotheses from 1970's are confronted with the recent developments in the field, we can conclude that the suggestions made nearly thirty years ago were essentially correct: the uptake, mediated by an active transport into neurons and glial cells, serves to control the extracellular concentrations of L-glutamate and prevents the neurotoxicity. The modern techniques of molecular biology may have provided additional data on the nature and location of the transporters but the classical neurochemical approach, using structural analogues of glutamate designed as specific inhibitors or substrates for glutamate transport, has been crucial for the investigations of particular roles that glutamate transport might play in health and disease. Analysis of recent structure/activity data presented in this review has yielded a novel insight into the pharmacological characteristics of L-glutamate transport, suggesting existence of additional heterogeneity in the system, beyond that so far discovered by molecular genetics. More compounds that specifically interact with individual glutamate transporters are urgently needed for more detailed investigations of neurochemical characteristics of glutamatergic transport and its integration into the glutamatergic synapses in the central nervous system. A review with 162 references.


Author(s):  
Stefano Vassanelli

Establishing direct communication with the brain through physical interfaces is a fundamental strategy to investigate brain function. Starting with the patch-clamp technique in the seventies, neuroscience has moved from detailed characterization of ionic channels to the analysis of single neurons and, more recently, microcircuits in brain neuronal networks. Development of new biohybrid probes with electrodes for recording and stimulating neurons in the living animal is a natural consequence of this trend. The recent introduction of optogenetic stimulation and advanced high-resolution large-scale electrical recording approaches demonstrates this need. Brain implants for real-time neurophysiology are also opening new avenues for neuroprosthetics to restore brain function after injury or in neurological disorders. This chapter provides an overview on existing and emergent neurophysiology technologies with particular focus on those intended to interface neuronal microcircuits in vivo. Chemical, electrical, and optogenetic-based interfaces are presented, with an analysis of advantages and disadvantages of the different technical approaches.


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