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Dive into the research topics where Andrew Greaves is active.

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Featured researches published by Andrew Greaves.


Angewandte Chemie | 2016

Plastic Antibodies for Cosmetics: Molecularly Imprinted Polymers Scavenge Precursors of Malodors

Sofia Nestora; Franck Merlier; Selim Beyazit; Elise Prost; Luminita Duma; Bérangère Baril; Andrew Greaves; Karsten Haupt; Bernadette Tse Sum Bui

Molecularly imprinted polymers (MIPs) are synthetic antibody mimics capable of specific molecular recognition. Advantageously, they are more stable, easy to tailor for a given application and less expensive than antibodies. These plastic antibodies are raising increasing interest and one relatively unexplored domain in which they could outplay these advantages particularly well is cosmetics. Here, we present the use of a MIP as an active ingredient of a cosmetic product, for suppressing body odors. In a dermo-cosmetic formulation, the MIP captures selectively the precursors of malodorous compounds, amidst a multitude of other molecules present in human sweat. These results pave the way to the fabrication of a novel generation of MIPs with improved selectivities in highly complex aqueous environments, and should be applicable to biotechnological and biomedical areas as well.


International Journal of Cosmetic Science | 2016

The effects of narrowbands of visible light upon some skin disorders: a review

Andrew Greaves

This review article focuses on clinical studies published in the fields of (i) photorejuvenation and anti‐ageing, (ii) oily or acne‐prone skin and related imperfections, (iii) skin pigmentation and lightening, (iv) dandruff and other Malassezia‐related skin disorders and (v) prevention and reversal of hair loss using non‐thermal, non‐ablative devices (principally light‐emitting diodes). It mainly focuses on clinical proof of performance and also on in vitro studies that support the clinical findings. The mode of action of narrowbands of visible light upon the skin is only briefly discussed since their biological effects have been previously reviewed.


Journal of Colloid and Interface Science | 2016

Mixed monolayers of alkane thiols with polar terminal group on gold: Investigation of structure dependent surface properties

Zahra Besharat; Deborah Wakeham; C. Magnus Johnson; Gustavo S. Luengo; Andrew Greaves; Inger Odnevall Wallinder; Mats Göthelid; Mark W. Rutland

Adsorption of thiols with cationic or anionic terminal group on gold has been studied from mixed solutions of 11-Amino-1-undecanethiol (AUT) and 3-Mercaptopropionic acid (MPA) using Quartz Crystal Microbalance with Dissipation (QCM-D), X-ray Photoelectron Spectroscopy (XPS), atomic force microscopy (AFM) and contact angles. The goal is to probe the nature of such layers, and the additivity or otherwise of the pH responsiveness, with a view to evaluate their suitability as smart materials. For each of the two pure (unmixed) cases, ordered molecular monolayers are formed with sulfur binding to gold and the alkane chain pointing out from the surface as expected. Adsorption from the thiol mixtures, however, leads to a more complex behaviour. The surface concentration of thiols from the mixtures, as determined by QCM-D, is considerably lower than for the pure cases and it reaches a minimum at a 3:1 MPA/AUT relative concentration in the solution. The XPS results confirm a reduction in adsorbed amount in mixtures with the lowest overall intensity for the 3:1 ratio. Monolayers formed from mixtures display a wettability which is much lower and less pH sensitive. Collectively these results confirm that for adsorption from mixed systems, the configuration is completely different. Complex formation in the mixed solutions leads to the adsorption of molecules parallel to the surface in an axially in-plane configuration. This parallel layer of thiols is mechanically relatively robust to nano-shaving based on AFM measurements. These results will have a significant impact on the design of biomimetic surface coatings particularly when mixtures of oppositely charged molecules are present on the surface, as is commonly the case in biological, proteinaceous surfaces (e.g. hair and skin).


Archive | 2007

Method of dyeing and lightening keratin materials in the presence of a reducing agent comprising a fluorescent disulphide dye

Nicolas Daubresse; Andrew Greaves; Henri Samain


Archive | 2005

Symetric diazo compounds containing 2-pyridinium groups and a linker being cationic or not, compositions containing them, process of dyeing and kit

Hervé David; Andrew Greaves; Nicolas Daubresse


Archive | 2005

Cationic symmetric 2-imidazolium diazo compounds with a cationic linking group,compositions comprising them, a dying process and kit thereof

Hervé David; Andrew Greaves; Nicolas Daubresse


Archive | 2005

Selected cationic diazo compounds, compositions comprising them as direct dye, methods for dyeing keratin fibres and kit

Andrew Greaves; Hervé David


Archive | 2005

Symmetrical diazo compounds with 3-pyridinium groups and cationic linker arm, compositions comprising same, dyeing method and device

Hervé David; Andrew Greaves; Nicolas Daubresse


Archive | 2004

Dyeing method for human keratinous fibers with lightening effect, particular fluorescent compound and composition comprising same

Andrew Greaves; Nicolas Daubresse; Xavier Radisson


Archive | 2005

Symmetrical diazo compounds containing 3-pyridinium groups and a non-cationic linker, compositions comrisisng them, method of colouring, and device

Hervé David; Andrew Greaves; Nicolas Daubresse

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