Effects of particulate matter on rates of membrane uptake of polynuclear aromatic hydrocarbons.

Investigations of the mechanism of particle-enhanced uptake of benzo [a] pyrene into model membranes and microsomes have been extended by studying the effects of particulates on the rates of uptake of four additional polynuclear aromatic hydrocarbons (PAH) into model membranes. Adsorption of dibenzo [a, h] anthracene, benzo [g,h,i] perylene, and 3-methylcholanthrene to the surface of particles resulted in enhanced rates of membrane uptake of these PAH. Adsorption to the fibrous asbestos minerals (chrysotile and anthophyllite) produced the greatest enhancement in membrane uptake rates compared to uptake from microcrystalline dispersions of the PAH. Adsorption of these PAH to nonfibrous minerals resulted in uptake rates intermediate between those of the asbestos-adsorbed and microcrystalline states. In contrast, adsorption of dibenzo-[c,g] carbazole to particles did not result in enhanced uptake. In this case, the rates of uptake in the absence and presence of particles were all extremely high, presumably as a result of the high water solubility of this PAH. The methods described in this paper permit characterization of particles-PAH mixtures in terms of the rate of PAH uptake into membranes.

Transport of a carcinogen, benzo[a]pyrene, from particulates to lipid bilayers: a model for the fate of particle-adsorbed polynuclear aromatic hydrocarbons which are retained in the lungs.

Fluorescence spectroscopic methods were used to investigate the effects of adsorption of benzo[a]pyrene to particulate matter on its rate of uptake into model membranes composed of dipalmitoyl L-alpha-phosphatidylcholine. From these experiments we conclude the following: 1. Adsorption of benzo[a]pyrene to four types of asbestos (anthophyllite, crocidolite, chrysotile, and amosite) and a variety of non-fibrous particles (hematite, silica, titanium dioxide, porous glass and talc) results in increased rates of membrane uptake when compared with aqueous suspensions of benzo[a]pyrene microcrystals. Benzo[a]pyrene was not released from carbon black. 2. Asbestos-adsorbed benzo[a]pyrene was transferred to the membranes most rapidly. 3. Adsorption of benzo[a]pyrene to the surface of the particles is necessary for its enhanced transport into membranes. That is, simple mixtures of benzo[a]pyrene microcrystals and particulates do not show enhanced transport. 4. Particle-enhanced transport of benzo[a]pyrene is not correlated with the effects of the particles on vesicle integrity, binding of vesicles to the particles, or the concentrations of either particles or vesicles. The rate limiting step for transport of benzo[a]pyrene into vesicles appears to be its rate of desorption from the surface of the particle. Following desorption, membrane uptake of benzo[a]pyrene is rapid.