Phosphorus (P) is the second important key plant nutrient after nitrogen. An adequate supply of P is therefore required for proper functioning and various metabolisms of plants. Majority of P in soils is fixed, and hence, plant available P is scarcely available despite the abundance of both inorganic and organic P forms in soils. A group of soil microorganisms capable of transforming insoluble P into soluble and plant accessible forms across different genera, collectively called phosphate-solubilizing microorganisms (PSM), have been found as best ecofriendly option for providing inexpensive P to plants. These organisms in addition to supplying soluble P to plants also facilitate the growth of plants by several other mechanisms, for instance, improving the uptake of nutrients and stimulating the production of some phytohormones. Even though several bacterial, fungal and actinomycetal strains have been identified as PSM, the mechanism by which they make P available to plants is poorly understood. This chapter focuses on the mechanism of P-solubilization and physiological functions of phosphate solubilizers in order to better understand the ecophysiology of PSM and consequently to gather knowledge for managing a sustainable environmental system. Conclusively, PSM are likely to serve as an efficient bio-fertilizer especially in areas deficient in P to increase the overall performance of crops.

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The nose-to-brain pathway has been proven to be a shortcut for direct drug delivery to the brain. However, whether and to what extent nanoparticles can be delivered through this passage is still awaiting validation with evidence. In this study, nose-to-brain transportation of nanoparticles is tracked via fluorescence bioimaging strategies using nanoemulsions (NEs) as model carriers. Identification of NEs in biological tissues is based on the on → off signal switching of a new type of environment-responsive embedded dyes, P2 and P4, and two conventional probes, DiR and coumarin-6 (C6), are embedded to represent the cargoes. Evidence for the translocation of NEs was collected either via live imaging or ex vivo histological examination in rats after nasal administration. Results suggest that NEs with a particle size of about 100 nm, either naked or coated with chitosan, have longer retention duration in nostrils and slower mucociliary clearance than larger ones. P2 signals, representing integral NEs, can be found in mucosa and trigeminal nerves for all size groups, whereas only weak P2 signals are detected in the olfactory bulb for chitosan-coated NEs of 100 nm. Confocal microscopy further confirms the translocation of integral 100 nm NEs in nasal mucosa and along the trigeminal nerve in decremental intensity. Weak signals of the P4 probe, also representing integral NEs, can be detected in the olfactory bulb but few in the brain. NEs as large as 900 nm cannot be transported to the olfactory bulb. However, the DiR or C6 signals that represent the cargoes can be found in significant amounts along the nose-to-brain pathway and finally reach the brain. Evidence shows that integral NEs can be delivered to the olfactory bulb, but few to the brain, whereas the cargoes can be released and permeated into the brain in greater amounts.

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Lipid nanovesicles are widely present as transport vehicles in living organisms and can serve as efficient drug delivery vectors. It is known that the size and surface charge of nanovesicles can affect their diffusion behaviors in biological hydrogels such as mucus. However, how temperature effects, including those of both ambient temperature and phase transition temperature (Tm), influence vehicle transport across various biological barriers outside and inside the cell remains unclear. Here, we utilize a series of liposomes with differentTmas typical models of nanovesicles to examine their diffusion behavior in vitro in biological hydrogels. We observe that the liposomes gain optimal diffusivity when theirTmis around the ambient temperature, which signals a drastic change in the nanovesicle rigidity, and that liposomes withTmaround body temperature (i.e., ∼37 °C) exhibit enhanced cellular uptake in mucus-secreting epithelium and show significant improvement in oral insulin delivery efficacy in diabetic rats compared with those with higher or lowerTm. Molecular-dynamics (MD) simulations and superresolution microscopy reveal a temperature- and rigidity-mediated rapid transport mechanism in which the liposomes frequently deform into an ellipsoidal shape near the phase transition temperature during diffusion in biological hydrogels. These findings enhance our understanding of the effect of temperature and rigidity on extracellular and intracellular functions of nanovesicles such as endosomes, exosomes, and argosomes, and suggest that matchingTmto ambient temperature could be a feasible way to design highly efficient nanovesicle-based drug delivery vectors.