Protein nanoparticles

To capitalize on the favorable characteristics of PNPs, improvements within PNP synthesis methods are being widely explored. Advancements or the development of new synthesis methods are desirable as existing methods (sonochemistry, thermal decomposition, and colloidal/ hydrothermal/microemulsion methods) contribute to systemic toxicity and are limited to hydrophilic drugs. As a result, recent advancements seek to overcome these challenges and achieve commercial-size production. In addition, newly developed PNP synthesis methods such as electrospray or desolvation provide a more sustainable approach as compared to traditional nanoparticle methods. == Types of protein ==

Numerous proteins are utilized in PNP synthesis. They are often sourced naturally from animal and plant sources. Accordingly, generally shared advantages of animal proteins include high biocompatibility, biodegradability, non-immunogenicity, drug loading efficiency, cell uptake, and easy and cost-effective production. Tables 2–4 below compile the common proteins used in PNP synthesis. The types of PNPs share similar physical properties such as high biocompatibility, non-immunogenicity, high drug efficiency, high biodegradability, and high cell uptake. Due to the abundance of proteins necessary for proper bodily function, the body has developed processes to update proteins into tissues and cells. PNPs take advantage of these natural processes to enhance their cellular uptake. This abundance and the natural sourcing subsequent purification of the proteins also reduce the immunogenic responses and produce low toxicity levels in the body. As the PNPs are degraded, the tissues assimilate the amino acids into energy or protein production. == Protein nanoparticle modifications ==

PNPs can be chemically modified to increase particle stability, reduce degradation, and enhance favorable characteristics. Crosslinking is a common modification that can utilize synthetic or natural cross-linkers. Natural cross-linkers are significantly less toxic than synthetic cross-linkers. Driving factors in the modification of PNPs stem from their surface properties (surface charge, hydrophobicity, functional groups, etc.). Functional groups can bind to tissue-specific ligands for targeted drug delivery. Functional ligands may include protein receptors, antibodies, and smaller peptides. The purpose of ligand binding is to direct the PNP to the target cells, thereby reducing systemic toxicity, and improving the retention and excretion of the PNP within tissues. The optimal ligand for PNP modification is dependent on the target cell. Modification of a PNP surface with ligands can be achieved through chemical conjugation, though chemical dyes for imaging and peptides for immune activation can also be attached [11,33,34]. One example is the ligand anti-human epidermal growth factor receptor 2 which targets breast cancer cells. The following provides additional applications of ligand modifications and their therapeutic applications [12]. In addition to chemical conjugation, genetic modification can facilitate direct attachment of the modifying protein monomers with the PNP surface. This results in a co-assembly and a solution to existing challenges with direct attachments or large proteins. Attaching large proteins to PNPs interferes with the self-assembly process and induces steric interactions. Though, smaller protein attachments are generally tolerated by protein NPs. A significant limitation to direct attachment via genetic modification of protein monomers is that it cannot accommodate the attachment of multiple components. Enzymatic ligation helps overcome this limitation by providing a site-specific covalent link to the PNP surface following PNP assembly. This strategy can also provide greater control over the density and ratios of attached proteins. The modification of VLPs is unique due to their nanocage architecture. PNPs with cage structures can fully encapsulate functional components in their interior, termed co-encapsulation. Drug encapsulation within VLP cages can occur through two processes. This first process occurs in-vitro and requires the disassembly of the cage and reassembling it with the presence of the drug components to be encapsulated [8]. Since loading efficiency is influenced through electrostatic interactions, the drug compounds cannot be fully encapsulated without interfering with the VLP cage self-assembly. Another process is the encapsulation of drug components in-vivo. This involves direct genetic attachment of the drug components to the interior of the VLP cage. This process guides drugs for encapsulation directly to the interior of the cage. == Therapeutic drug delivery applications ==

Due to PNPs' breadth of favorable pharmacokinetic properties such as high biocompatibility, high biodegradability, high modifiability, low toxicity, high cell uptake, and a fast excretion rate, PNPs are prime candidates for anti-cancer therapy. Previous anticancer therapies relied on the enhanced permeability effect to passively accumulate within tumors. This resulted in greater toxicity due to higher concentrations required to achieve critical drug efficacy levels. Newer strategies allow PNPs to actively target the tumor microenvironment via the attachment of ligands and site-specific protein receptors. Active targeting decreases the total concentration of drugs required to deliver an effective dose, thereby reducing systemic side effects. In addition to active tumor targeting, PNPs can also be engineered to respond to changing external environments such as pH, temperature, or enzyme concentration. The tumor microenvironment is slightly acidic, so PNPs can be engineered to only release their drug cargo under specific tumor physiological conditions. Other applications include vaccine development through VLPs carrying immunogenic components. Since VLPs are not carrying any attenuated genetic material, these vaccines pose a safer alternative, especially for the immunocompromised or elderly. PNPs may also treat neurological diseases as they can cross the blood-brain barrier [28]. Lastly. PNPs may find applications within ophthalmic drug delivery as PNPs have a significantly longer circulation time in the eye than eye drops. == Drug delivery challenges and regulations ==

Despite numerous pharmacokinetic advantages of PNPs, there remain several critical challenges to their clinical translation. Only two PNPs have been FDA-approved, despite over 50 PNP formulations to date (2022). The two FDA-approved drugs include Abraxane, an albumin nanoparticle carrying paclitaxel used for breast cancer, non-small cell lung cancer, and pancreatic cancer treatment. The second FDA-approved PNP is Ontak, a protein conjugate carrying L-2 and Diphtheria toxin used for cutaneous T-cell lymphoma. The two approved formulations are summarized in Table 5 below. The low approval rate of PNPs is due to limited existing control over drug encapsulation and the pharmacokinetic variability between PNP batches. Balancing both the repeatability of these two properties and their relative interactions is important because it ensures the predictability of their clinical outcomes, greater patient safety, and that protein loading does not interfere with the PNP's properties. Another limitation surrounds the cost and ability of large-scale production. Many synthesis methods that can deliver greater homogeneity between produced nanoparticles are also more costly options or cannot achieve mass production. This limitation is compounded by the lower yields of PNP manufacturing. This limits the availability of PNPs to broad clinical adoption [20,29]. == References ==