Crystalline materials are of crucial importance to the pharmaceutical industry, as a large number of APIs are formulated in crystalline form, occasionally in the presence of crystalline excipients. Owing to their multifaceted character, crystals were found to have strongly anisotropic properties. In fact, anisotropic properties were found to be quite important for a number of processes including milling, granulation and tableting. An understanding of crystal anisotropy and an ability to control and predict crystal anisotropy are mostly subjects of interest for researchers. A number of studies dealing with the aforementioned phenomena are grounded on over-simplistic assumptions, neglecting key attributes of crystalline materials, most importantly the anisotropic nature of a number of their properties. Moreover, concepts such as the influence of interfacial phenomena in the behaviour of crystalline materials during their growth and in vivo, are still poorly understood. The review aims to address concepts from a molecular perspective, focusing on crystal growth and dissolution. It begins with a brief outline of fundamental concepts of intermolecular and interfacial phenomena. The second part discusses their relevance to the field of pharmaceutical crystal growth and dissolution. Particular emphasis is given to works dealing with mechanistic understandings of the influence of solvents and additives on crystal habit. Furthermore, comments and perspectives, highlighting future directions for the implementation of fundamental concepts of interfacial phenomena in the rational understanding of crystal growth and dissolution processes, have been provided.
A method for screening compatible buffer conditions for both DNA origami and protein crystallisation and studied how protein crystallisation buffer conditions notably cations, buffering agents, precipitants, and pH, influenced the stability of tubular DNA origami.
A nanochannel with a shutter at one end was built by DNA nanotechnology. Using DNA hybridization the shutter could be opened or closed, influencing the transport of materials through the channel. This process was visualized by an enzyme cascade reaction occurring in the structure.
This
study reports the first experimental evidence of DNA origami as a
seed resulting in the increase in probability of protein crystallization.
Using the DNA origami constructed from long single-stranded M13 DNA
scaffolds folded with short single-stranded DNA staples, it was found
that the addition of the DNA origami in concentrations of 2–6
nM to mixtures of a well-characterized protein (catalase) solution
(1.0–7.0 mg/mL) resulted in a higher proportion of mixtures
with successful crystallization, up to 11× greater. The improvement
in crystallization is evident particularly for mixtures with low concentrations
of catalase (<5 mg/mL). DNA origami in different conformations
of a flat rectangular sheet and a tubular hollow cylinder were examined.
Both conformations improved the crystallization as compared to control
experiments without M13 DNA or nonfolded M13 DNA but exhibited little
difference in the extent of protein crystallization improvement. This
work confirms the predictions of the potential use of DNA origami
to promote protein crystallization, with potential application to
systems with limited protein availability or difficulty in crystallization.
A new approach to the development of MOF materials with low water affinity is presented using siloxane-derived linkers. The low water affinity is conferred by the linker without the requirement of any post-synthetic processing apart from activation.
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