cell symmetry
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Biomolecules ◽  
2020 ◽  
Vol 10 (4) ◽  
pp. 642 ◽  
Author(s):  
Donald A. Tomalia ◽  
Linda S. Nixon ◽  
David M. Hedstrand

This article reviews progress over the past three decades related to the role of dendrimer-based, branch cell symmetry in the development of advanced drug delivery systems, aqueous based compatibilizers/solubilizers/excipients and nano-metal cluster catalysts. Historically, it begins with early unreported work by the Tomalia Group (i.e., The Dow Chemical Co.) revealing that all known dendrimer family types may be divided into two major symmetry categories; namely: Category I: symmetrical branch cell dendrimers (e.g., Tomalia, Vögtle, Newkome-type dendrimers) possessing interior hollowness/porosity and Category II: asymmetrical branch cell dendrimers (e.g., Denkewalter-type) possessing no interior void space. These two branch cell symmetry features were shown to be pivotal in directing internal packing modes; thereby, differentiating key dendrimer properties such as densities, refractive indices and interior porosities. Furthermore, this discovery provided an explanation for unimolecular micelle encapsulation (UME) behavior observed exclusively for Category I, but not for Category II. This account surveys early experiments confirming the inextricable influence of dendrimer branch cell symmetry on interior packing properties, first examples of Category (I) based UME behavior, nuclear magnetic resonance (NMR) protocols for systematic encapsulation characterization, application of these principles to the solubilization of active approved drugs, engineering dendrimer critical nanoscale design parameters (CNDPs) for optimized properties and concluding with high optimism for the anticipated role of dendrimer-based solubilization principles in emerging new life science, drug delivery and nanomedical applications.


2019 ◽  
Vol 44 (21) ◽  
pp. 5169
Author(s):  
Ning Wang ◽  
Matthias Zeisberger ◽  
Uwe Hübner ◽  
Markus A. Schmidt

2015 ◽  
Vol 79 (2) ◽  
pp. 485-495 ◽  
Author(s):  
Cristian Biagioni ◽  
Stefano Merlino ◽  
Elena Bonaccorsi

AbstractThe name 'tobermorites' includes a number of calcium silicate hydrate (C-S-H) phases differing in their hydration state and sub-cell symmetry. Based on their basal spacing, closely related to the degree of hydration, 14, 11 and 9 Å compounds have been described. In this paper a new nomenclature scheme for these mineral species is reported. The tobermorite supergroup is defined. It is formed by the tobermorite group and the unclassified minerals plombièrite, clinotobermorite and riversideite. Plombièrite ('14 Å tobermorite') is redefined as a crystalline mineral having chemical composition Ca5Si6O16(OH)2·7H2O. Its type locality is Crestmore, Riverside County, California, USA. The tobermorite group consists of species having a basal spacing of ∼11 Å and an orthorhombic sub-cell symmetry. Its general formula is Ca4+x(AlySi6–y)O15+2x–y·5H2O. Its endmember compositions correspond to tobermorite Ca5Si6O17·5H2O (x = 1 and y = 0) and the new species kenotobermorite, Ca4Si6O15(OH)2·5H2O (x = 0 and y = 0). The type locality of kenotobermorite is the N'Chwaning II mine, Kalahari Manganese Field, South Africa. Within the tobermorite group, tobermorite and kenotobermorite form a complete solid solution. Al-rich samples do not warrant a new name, because Al can only achieve a maximum content of 1/6 of the tetrahedral sites (y = 1). Clinotobermorite, Ca5Si6O17·5H2O, is a dimorph of tobermorite having a monoclinic sub-cell symmetry. Finally, the compound with a ∼9 Å basal spacing is known as riversideite. Its natural occurrence is not demonstrated unequivocally and its status should be considered as “questionable”. The chemical composition of its synthetic counterpart, obtained through partial dehydration of tobermorite, is Ca5Si6O16(OH)2. All these mineral species present an order-disorder character and several polytypes are known. This report has been approved by the International Mineralogical Association Commission on New Minerals, Nomenclature and Classification.


2015 ◽  
Vol 106 (9) ◽  
pp. 091905 ◽  
Author(s):  
Paolo Celli ◽  
Stefano Gonella
Keyword(s):  

Nature ◽  
2015 ◽  
Vol 518 (7538) ◽  
pp. 232-235 ◽  
Author(s):  
Julija Krupic ◽  
Marius Bauza ◽  
Stephen Burton ◽  
Caswell Barry ◽  
John O’Keefe

Phytotaxa ◽  
2014 ◽  
Vol 178 (2) ◽  
pp. 128 ◽  
Author(s):  
Jonathan Charles Taylor ◽  
BALASUBRAMANIAN KARTHICK ◽  
J. PATRICK KOCIOLEK ◽  
CARLOS E. WETZEL ◽  
CHRISTINE COCQUYT

In this paper we describe Actinellopsis murphyi gen. et spec. nov. a small heteropolar and dorsiventral diatom from a seep habitat in Zambia. This novel taxon has the chief distinguishing characteristic, along with its cell symmetry, of having the raphe positioned wholly in the valve face and not extending onto the mantle. It is further placed within the Peroniaceae as it possesses a straight raphe on the valve face and rimoportulae, and the frustules are heteropolar with regard to the length of the raphe. We also transfer the fossil diatom Actinella giraffensis to Actinellopsis as the morphological characteristics of this taxon are consistent with those of the generitype.


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