A series of nanoparticles is prepared via layer‐by‐layer assembly of oppositely charged, synthetic biocompatible polyamidoamine polymers as potential carriers. Particle size, surface charge and internal chain mobility are quantified as a function of the polymer type and number of layers. The effect of addition of surfactant is examined to simulate the effects of nanoparticle dissolution. The cyctotoxicity of these particles (in epithelia and murine cell lines) are orders of magnitude lower than polyethyleneimine controls. Stable nanoparticles may be prepared from mixtures of strongly, oppositely charged polymers, but less successfully from weakly charged polymers, and, given their acceptable toxicity characteristics, such modularly designed constructs show promise for drug and gene delivery.
Hollow multilayer microcapsules made of aliphatic poly(urethane‐amine) (PUA) and sodium poly(styrene sulfonate) (PSS), templated on PSS‐doped CaCO3 particles, are prepared for pH‐/thermally responsive drug delivery. The electrostatic interaction and hydrogen bonding under weak‐acid conditions between aliphatic PUA and PSS contribute to the formation of multilayer microcapsules. Scanning electron microscopy (SEM) results demonstrate an obvious variation of the hollow multilayer microcapsules in response to changes in temperature and pH value. Drug‐release behaviors using DOX as a model drug demonstrate that the drug release increases on decreasing the pH value because of the interaction weakness between aliphatic PUA and PSS in acidic conditions. Moreover, the drug release is higher at 55 °C than that at 37 °C for the sake of the shrinkage of aliphatic PUA above its lower critical solution temperature (LCST).
SPE method is a very popular technique, and is commonly used for the prepurification, concentration, and isolation of different organic compounds from variable matrices. In this work, the optimization of SPE process was carried out. The breakthrough volume of solid sorbents based on octadecylsilane was determined and three methods were compared: (1) calculation one – the breakthrough volume was calculated using retention factor k determined with micro‐TLC method, frontal analysis – (2) breakthrough volume was determined as volume of whole elution peak, and (3) breakthrough volume was determined as the center of peak gravity. For calculation method, the k values of key estrogens and progestogens were derived from the micro‐TLC experiment reported previously. By combining these three methods, we can point the start of elution, the maximum concentration of analyte in eluate, and the whole eluent volume, which is necessary to achieve an appropriate selectivity and high extraction recovery. Proposed calculation method allows to estimate the beginning of the steroid peak, when the analyte appears in the eluate flowing from the sorbent. Such observation advances the SPE optimization protocol that was described before and was based on the correlation between raw kSPE and kmicro‐TLC data. 相似文献
The effects of ethanol on the thickness and ionization of adsorbed polymer layer on pigment were investigated. The results showed that the thickness of adsorbed polymer layer decreased with the increase of the ethanol concentration, and then the pigment particles aggregated when the concentration of ethanol is higher than 40%. The zeta potentials became more negative with the increasing of the ethanol concentration, and then changed reversely when the ethanol concentration was higher than 16%. The thickness and structure of adsorbed polymer layer on the particle determined the stability of pigment dispersion. 相似文献
The effect of replacing the conventional uniform macroion surface charge density with discrete macroion charge distributions on the structure of electric double layer (EDL) of a spherical macroion has been investigated by Monte Carlo (MC) simulations. Two discrete models have been investigated in addition to the central macroion charge: point charges localized on the macroion surface and finite-sized charges protruding into the solution. Both models have been studied with fixed and mobile macroion charges. The radial functions of local densities and electrostatic potential in EDL, are calculated and compared to the results obtained for the central macroion charge distribution. It is concluded that the model of charge distribution significantly affects the EDL structure close to the macroion, while the effect is much weaker at larger distances. With point charges localized on the macroion surface, counterions become stronger accumulated to the macroion, as a result the absolute values of surface potential ?0 and zeta ξ potential are decreased. With protruding charges, the excluded volume effect dominates over the increased correlation ability; hence the counterions are less accumulated near the macroions and the absolute values of ?0 and ξ potentials are increased. 相似文献
Aqueous ethylene glycol (ethane 1,2 diol) as a green mobile phase has been used for thin layer chromatographic (TLC) studies of cationic surfactants on alumina layers. Nineteen solvent systems were used to examine the mobility of the surfactants and to discover the best TLC system for the selective separation of dodecyl trimethylammonium bromide (DTAB) from multi-component mixture of other surfactants. Among the TLC systems studied, M3 (ethylene glycol: water, 8:2) was best for achieving the selective separation of DTAB from multi-component mixture of other surfactants because in this mobile phase mobility of all surfactants except DTAB were insignificant. Effect of organic additives in aqueous ethylene glycol mobile phase on the mobility of surfactants was examined. The results obtained on laboratory made alumina TLC plates and commercially available precoated alumina HPTLC plates were compared. The lower limits of detection of DTAB, CPC, CTAB, HDTAC, and TTAB were 0.02, 0.05, 0.04, 0.06, or 0.08 µg per zone respectively. The resolution of mixture of cationic surfactants was also examined in the presence metal cations as an impurity in the analyzed sample. 相似文献
Here, we demonstrate excellent liquid crystal (LC) vertical alignment without using an alignment layer printing process by introducing octadecyltrichlorosilane (OTS) into the LC mixture. Further, we investigated the alignment mechanism by analysing the surfaces of the substrates. The optimum concentration of OTS was found to be about 0.03wt%, which is 1/100 of that in the previously reported polyhedral oligomeric silsesquioxane (POSS)–LC system. Moreover, the OTS–LC system exhibited a more stable LC alignment compared with the POSS–LC system. These differences may arise from the different strengths of surface–dopant interactions; that is, the covalent bond in the OTS–LC system and the van der Waals interactions in the POSS–LC system. We also demonstrated that the method can be used in a capillary tube, which may serve as a new method facilitating the application of LCs with curved surfaces. 相似文献