Earlier reports showed the expression of Tf receptor (TfR) in all nucleated cells and the BBB and overexpression in a variety of tumors (Nabi et al., 2018a). TfR is overexpressed in brain neurons, capillary endothelium cells, and choroid plexuses (Sundaram et al., 2009; Choudhari et al., 2021). Tf is a glycoprotein that binds to the iron in the blood and delivers it to the brain via TfR present on the BBB (Sharma et al., 2016a; Choudhari et al., 2021). The transport of Holo-Tf from blood to the brain and apo-Tf from the brain to blood is mediated by the TfR (Liu et al., 2013). Transport of Tf to the brain can be achieved via a receptor-mediated endocytosis mechanism. The cellular internalization of Tf-conjugated NPs to the targeted cells (brain neurons) can result in significant enhancement of drug therapeutic efficacy, thus reducing administered drug dose and dosing frequency. Tf conjugation provides site-specific delivery of the drugs, thus reducing drug-related adverse effects and peripheral drug toxicity (Liu et al., 2013; Nabi et al., 2018b). Some studies that target TfR for delivering drugs to the brain are mentioned below. Nabi and associates demonstrated the enhanced brain delivery of Tf-conjugated chitosan NPs in the management of neurodegenerative disorders (Nabi et al., 2020). Tf can be used for the transport of metallic particles; for example, gallium has widespread use as a targeted drug delivery carrier, that is, via the Tf pathway. Also, in DNA replication, the Tf role is reported (Vijayalakshmy et al., 2019). Tf (MAB) monoclonal antibody (OX26 or R17-217) or protein can be conjugated to the NP surface. Reportedly, the monoclonal antibody conjugated to Tf binds to different sites at TfRs in comparison to TfR protein; thus, there is a very low chance of interference of MAB-targeted Tf-NPs with endogenous Tf in circulation. Thus, to curtail the limitations of Tf as a drug delivery vehicle, TfR-targeted antibodies were used. i.e., 8D3 anti-mouse TfR monoclonal antibody (8D3), anti-rat TfR monoclonal antibody (OX26), and R17-217 (Sharma et al., 2016).

(OX26) Anti-TfR antibody is mainly used in brain targeting in the management of brain glioma and binds to the TfR epitope; thus, it does not compete with the natural binding site of Tf. It is basically an anti-rat TfR monoclonal antibody and does not bind to human TfR; thus, the clinical implication of this technology is impossible (Gaillard et al., 2005; Liu et al., 2013). It is transported to rats’ TfR via receptor-mediated transcytosis (Cano et al., 2020). OX26 is one of the most exploited antibodies of the Tf family due to its higher success in brain delivery (Nabi et al., 2018b). In vitro and in vivo studies revealed better brain delivery across the BBB of OX26-modified PEG liposomes with a lower tumor value and increased survival time (Yue et al., 2014).

R17-217 anti-TfR antibody also has the potential to enhance gene transfection and drug delivery, as it mediates NP transport across the BBB (Gao, 2016). It is a monoclonal antibody that binds specifically to TfRs via receptor-mediated endocytosis. A study conducted by Kang and associates summarized an increased penetration and uptake of docetaxel (DTX) liposomes co-modified with muscone and R17-217 into tumor spheroids. Also, in vivo results reported increased brain targeting and survival rate in tumor-bearing nude mice (Kang et al., 2020).

Apo-Tf is related to the Tf family and possesses Tf-like characteristics when it is unbound to iron. It is a single-chain glycoprotein that exists in the plasma as mono or differic Tf, having a high affinity towards ferric iron with two nonidentical iron-binding sites. Choi and Park developed DTX nanocrystals and modified them with human apo-Tf to improve the cytotoxicity and cellular uptake of DTX (Choi and Park, 2017). Infusion of Apo-Tf might minimize the oxidative damage by binding to the released iron during radiotherapy (Vijayalakshmy et al., 2019). It was found from the literature that administration of Tf via nasal route is a fruitful approach that provides protective action to neurons in hypoxic–ischemic management; the study was implicated on mouse and rat models.

Lactoferrin (Lf) a cationic glycoprotein (iron-bounded) that belongs to the Tf family and exhibited higher activity in comparison to OX26 and Tf for transferring active therapeutics across the BBB (Gao, 2016). Lf exhibits antibacterial, antiviral, antimicrobial, and antitumor biological functions. It crosses the BBB via transcytosis pathways within endothelial cells of the brain capillary (Tomitaka et al., 2015). Lf-modified NPs have been widely used for targeting brain glioma. Li and associates developed Lf-modified PEG–polylactide (PEG-PLA) NPs of shikonin to target the glioma cells via receptor-mediated endocytosis. Modified NPs revealed sustained release of more than 72 h and higher brain concentrations in vivo than free shikonin NPs and shikonin (Li et al., 2017). The report suggested that in targeting brain glioma using magnetic particle imaging, Lf-modified iron oxide NPs can be used as tracers (Tomitaka et al., 2015).

Insulin receptor antibody exhibits very high BBB-penetrating efficiency compared to TfR antibodies. The insulin receptor is abundantly present in the brain (hypothalamus, hippocampus, cerebral cortex, and olfactory bulb). In CNS, these receptors have effective action in neuronal survival, homeostasis, and reproductive endocrinology (Choudhari et al., 2021). Insulin is an endogenous protein that is transported via receptor-mediated transcytosis to the brain and specifically acts on insulin receptors (Cano et al., 2020). The transport of insulin across the brain parenchyma can be influenced or increased by pro-inflammatory factors like tumor necrosis factor and interleukin-1 (Pomytkin et al., 2018).

Cell-penetrating peptides (CPPs) are amphipathic or small cationic cargo having the ability to transport molecular molecules like (oligonucleotides, peptides, proteins, nanoparticles (NPs), liposomes, etc.) to the innermost cells. CPPs can cross the cell membrane via energy-independent or receptor-mediated processed, and without compromising their bioavailability, they efficiently internalize the associated biomolecules to the cells. They have been exploited widely to establish their efficiency in the management of brain-related diseases. Various kinds of CPPs used in the medical domain are penetratin, transactivator of transcription peptide (TAT), and poly-l-arginine (Sharma et al., 2016a; Nabi et al., 2018a). Currently, about 1,850 kinds of CPP sequences are available on the CPP site 2.0 database. The exact mechanism of CPP cellular uptake remains controversial; however, the general mechanism for CPP uptake is considered to be endocytosis or non-endocytosis direct translocation (Xie et al., 2020). They can transport therapeutic agents across the BBB through adsorptive-mediated transcytosis and demonstrated BBB translocation in submicromolar concentrations without generating cytotoxic effects (Sharma et al., 2016b; Xie et al., 2020). A cell-penetrating mitochondrion-targeting peptide was designed computationally to transduce human metallothionein 1A (hMT1A) (antioxidant protein) into mitochondria, which in the PD mouse model rescued dopaminergic neuronal degeneration and movement impairment (Kang et al., 2018).

It is a specific receptor that is present on the BBB and helps in selective and specific delivery of drug lipoprotein complex. It is related to high-density lipoprotein, very-low-density lipoprotein, and specifically a 34-kDa protein class that helps in the transportation of lipids and cholesterol across the BBB (Bu, 2009). Apo-E is transported via the receptor-mediated endocytosis mechanism to the endothelial low-density lipoprotein (LDL) receptor (Cano et al., 2020). Human Apo-E differs both functionally and structurally from mouse Apo-E. It modulates multiple mechanistic pathways (e.g., cholesterol/lipid homeostasis, glucose metabolism, synaptic function, neurogenesis, neuroinflammation, and amyloid-β aggregation) in CNS, which affects cognition (Tai et al., 2016). A 1.8-fold increase in cellular uptake of palmitate solid lipid NPs (SLNs) modified with APO-E and a 1.9-fold increase in DSPE-Apo-E-modified SLNs were reported by Neves and associates (Neves et al., 2017). A significant enhancement in brain uptake via Apo-E NPs was observed by Hartl and associates (Hartl et al., 2021).

It is categorized as LRP1, which is present on the BBB and brain, whereas LRP2 protein is specifically found only in the brain. In vitro BBB model and in situ bovine brain perfusion of Aprotinin (LRP) ligand showed higher transcytosis across capillary endothelial cells of the brain (Harilal et al., 2020). Both LRPs are closely or structurally related to the gene family of the LDL receptor. They are multiligand scavengers and multifunctional and signaling receptors (Gaillard et al., 2005). They are transported to the endothelial LDL receptor via receptor-mediated endocytosis (Cano et al., 2020).

Epidermal growth factor receptor (EGFR) is a transmembrane glycoprotein receptor whose extracellular domain acts as a receptor, while the intracellular domain acts as tyrosine kinase with a high affinity towards EGF (Nabi et al., 2018a). In cancer cells, they are expressed highly, and more than 40% are expressed in glioblastoma (GBM), indicating their role in the pathogenesis of GBM (Mortensen et al., 2013). About 25% of GBM is characterized by EGRFR mutant expressions that are defective of extracellular ligand-binding domain. In preclinical and clinical trials, lapatinib, gefitinib, and erlotinib have been tested for malignant glioma treatment (Ferraris et al., 2020a). For the treatment of head, neck, and metastatic colorectal cancers, cetuximab is an EFR-targeting antibody approved by the Food and Drug Administration (FDA) (Desnoyers et al., 2013). Mouse anti-human EGFR nimotuzumab antibodies in clinical trials were employed for recurrent high-grade glioma patients (Ferraris et al., 2020a).

As the name suggests, the “targeting approach” reflects the ability of the drug delivery system to target the specific site to achieve therapeutic effects. But the plethora of several features influencing the effectiveness of the targeting systems hinders the achievement of the therapeutic efficacy of these systems. Insufficient targets, in addition to the choice of the target with different alignments to the interruption necessities, cause difficulty in this process. Moreover, for sufficient uptake of the drug by cells, choosing suitable target epitopes is required to regulate the approachability of attaching drug conjugates with bulkier drug carriers. However, designing of these targeting systems must acclimatize numerous physiological variables including the flow of blood, status of the disease, and the architecture of the tissues by lodging physicochemical constraints including the structure of the nanocarriers, composition of the carriers of the drugs, and how to put them into work (Muro, 2012). The applications of the targeted delivery system are much more associated with some hurdles to the effectual delivery of the drug. There is an occurrence of low bioavailability of the drugs at the target site when delivered using these carriers; these systems are prone to opsonization and thereby suffer from unwanted reticuloendothelial system (RES) uptake directly affecting the drug efficacy. In addition to these, these carriers voluntarily erupt from circulation via vascular gaps or any defect credited in process angiogenesis that is characteristic of tumor sites (Cukierman and Khan, 2010).

Apart from the challenges associated with the targeted drug delivery systems, there are some benefits that these delivery systems offer including maintenance of the drug level in the plasma and tissues thereby evading any harmful effect of drugs on the healthy cells (Cukierman and Khan, 2010; Pattni and Torchilin, 2015). Moreover, these systems are preferred much for the drugs belonging to BCS class IV. A targeted drug delivery system helps in enhancing the absorption of the drug or combination of the drugs at the diseased site. In comparison with conventional drugs, this system is highly specific and desirable, thus increasing the therapeutic profile of the drugs (Rani and Paliwal, 2014).

These NPs or nanomedicine have tremendous properties like antimicrobial activity, anti-insecticidal activity, and nontoxicity; hence they can be used in the diagnosis of life-threatening diseases. Cerium NPs can help in combating AD and cancer, but their use is limited due to the lack of stability in living organisms (Singh et al., 2021). Similarly, iron oxide NPs showed great properties in GBM treatment (Kievit and Zhang, 2011; Tomitaka et al., 2015). Cobalt NPs have good magnetic, optical, mechanical, and chemical properties and are successfully used in MRI. Moreover, cerium oxide NPs have excellent antioxidant properties and can be used in the treatment of neurodegenerative disorders and ischemic stroke/cerebral stroke (Rzigalinski et al., 2006; Singh et al., 2021). Selenium was also reported to reduce the risk of neurodegenerative diseases in various animal models. However, there is a lot of research needed to develop metal and metal oxide NPs to treat CNS disorders efficiently (Singh et al., 2021).

To reach the target site, extravasation is the first step for NPs in circulation, which can be altered by NP size and shape, as smaller NPs more easily cross the capillary walls than larger NPs. NPs show size-dependent distribution across the organs (Mitchell et al., 2021). If only considering the size, then studies also supported that NPs within 100 and 200 nm in size are more suitable due to their prolonged blood circulation and low uptake by the mononuclear phagocyte system, and also they have the potential to cross the BBB (Kulkarni and Feng, 2013; Wei et al., 2018). Single-walled carbon nanotubes with 30-nm size showed both higher nuclear and cellular internalization than 50 nm (Donkor and Tang, 2014). Most studies performed in vitro demonstrate that NPs with the size range of 10–60 nm have higher cellular uptake in nonphagocytic cells irrespective of their surface charge and composition (Hoshyar et al., 2016). The shape of NPs has a significant influence on their biodistribution, clearance, and cellular internalization. Studies demonstrated that NPs with worm-shape exhibit very long circulation than other shapes (Wei et al., 2018). The report suggested higher cell adhesion efficiency of elongated NPs due to their higher surface area, which helps in multivalent interaction of particles with the cell surface, whereas spherical NPs have a limited number of binding sites and smaller contact area due to their curved shape (Agarwal et al., 2013). In vitro and in vivo studies demonstrated higher efficiency and affinity of rod-shaped NPs to endothelial cells. Also, ellipsoidal NPs demonstrate lower cellular uptake in comparison to spherical NPs (Salatin et al., 2015). Nowak and associates in their studies showed size-dependent transport of NPs through endothelial cells. It was found that the particles with 200-nm spheres have 3-fold higher permeation than 100-nm spheres, and 100- and 10-fold lower permeation of 500-nm NPs than 200- and 100-nm spheres, respectively. Nontargeted rods showed lower adhesion on the synthetic surface than spheres. Also, the data revealed that rods shaped NPs have higher transport across the brain endothelium than spheres. Stiff particles showed higher transport than their soft counterparts (Nowak et al., 2019).

NPs have limited application in brain tumors, as they have insufficient retention and accumulation within the tumors due to leaky vasculature and restricted target specificity, as the exclusivity of known receptors is very less in brain tumors. Also, the inability of NPs to traverse the BBB in brain glioma is a limitation in delivering the drugs to the brain (Jain, 2012; Masserini, 2013; Belykh et al., 2020). Maintaining the safety, efficacy, and tolerability of NPs into the brain is a major challenge (Cano et al., 2020). The most prominent challenges linked to NPs are their industrial scale-up and complex regulatory approval. However, to evaluate the therapeutic potential of NPs in neurodegenerative diseases, clinical trials have been started (El-Say and El-Sawy, 2017; Cano et al., 2020). The particle size and charge of NPs affect the brain delivery of NPs, as particles with 100–200 nm in size are considered to be optimum for brain delivery (Shakeri et al., 2020). So the development of optimum size NPs is also a challenging task. In the extracellular matrix, the diffusion of NPs is limited due to their large size (Barua and Mitragotri, 2014).

Figure 4 summarizes the application of NPs in brain delivery (Nair et al., 2016; El-Say and El-Sawy, 2017; Ferraris et al., 2020b; Cano et al., 2020).

✓ They can be easily transported across the BBB without any damage to the BBB

The amine-NH₂ and hydroxyl-OH group present in the chitosan are active sites for modification. The modification will impart solubility, stability, and bioadhesion to the NPs. The most commonly employed techniques for the preparation of chitosan polymers are blending, curing, and graft co-polymerization. Positively charged chitosan NPs interact with negatively charged mucous membrane and release the drug (Mohammed et al., 2017). Adsorption of chitosan is a physiochemical phenomenon in which the polymeric material chains are deposited on the NP surface. The interaction or covalent bonding between functional groups of chitosan and NPs can be obtained via different reactions before or after NP preparation, which depends on the chemical properties of the materials and the method of synthesis. The modification of NPs with chitosan will enhance its brain delivery (Prado-Audelo et al., 2020). Figure 5 summarizes the strategies of NP modification with chitosan for drug delivery.

PD is a growing and appalling neurodegenerative condition of the brain or CNS. It is mostly identified by dopaminergic neuron degeneration in the nigrostriatal bundle and midbrain region, which connects the pars compacta of the substantia nigra along with the dorsal striatum (Paul and Yadav, 2020). Poor balance, reduced motor control, tremors, and muscle stiffness are the primary symptoms of PD. The medication (levodopa, MAO-B inhibitors, dopamine, etc.) used for PD treatment aims to reduce the dopaminergic deficit. Though these medications dominate the treatment practice, the conventional dosage forms of these drugs suffer from enzymatic degradation, peripheral side effects, and low therapeutic efficacy. So novel therapies such as PNPs have gained much attention by the researchers for the treatment of PD patients, which provide the target-specific delivery, enhance therapeutic drug efficacy, and omit drug peripheral toxicity (Gan et al., 2019; Paul and Yadav, 2020). Various PNP-based formulations developed by the researchers for the treatment of PD are mentioned hereafter.

The poor oral bioavailability of ginkgolide B (GB) limits its clinical efficacy in PD treatment despite having good neuroprotective action. PEG-PCL NPs of GB were engineered by antisolvent precipitation and stabilization-based technique. PEG-PCL (20 mg/ml of acetone) and 2 ml of GB were mixed with 10 ml of dH₂O having F68 (0.5 mg/ml) stabilizer with constant stirring at 1,000 rpm and room temperature. Similarly, C-6-NPs were prepared by substituting GB for C6 under dark conditions. The study conducted in Madin–Darby canine kidney cells depicted that the prepared NPs were effectively taken by the body via multiple nonspecific mechanisms including clathrin-mediated endocytosis, micropinocytosis, and caveolae/lipid raft-mediated endocytosis. NPs of GB showed the ability to transport across chorion, the BBB, gastrointestinal (GI) barrier, and blood–retinal barrier (BRB) in a zebrafish model. Pharmacokinetics data revealed the enhanced uptakes (11.03-fold) of GB in rats’ brains and plasma after oral administration as compared to free GB. Figure 6 shows the pharmacokinetic profiles of free GB and NPs of GB in the rat brain and plasma. Also, GB-NPs demonstrate higher therapeutic efficacy and reduced GB toxicity in the murine PD model as compared to free GB (Zhao et al., 2020).

Author’s opinion: Thus, the above study demonstrates that PEG-coated PNPs might be potential vehicles for targeting therapeutic active molecules to the brain to treat PD.

In PD, the excess deposition of iron may often result in dopaminergic neuron necrosis and oxidative stress. To decrease oxidative stress in PD striatum and substantia nigra of mice, You and associates used deferoxamine (DFO) polymeric NPs modified with rabies virus glycoprotein (RVG)29 as brain targeting peptide for intracerebral delivery of DFO. RVG29- and DFO-loaded NPs exhibited mean diameter of 168.8 ± 1.9, −27.40 ± 0.71 zeta potential, uniform and smooth morphology represented by transmission electron microscopy (TEM), and about 75% of in vitro drug release in 24 h (Figure 7). The study revealed the penetrations of NPs through the BBB via receptor-mediated endocytosis mechanism. NPs showed a significant decrease in oxidative stress and iron content and reversal in neurobehavioral deficits without any toxic effects to the brain and other organs in the PD mouse model. The study holds promising results for DFO delivery to the brain and utilizing iron chelation therapy for the treatment of PD (You et al., 2018).

Neuroinflammation occurs in the subventricular zone where the proliferation of neural stem cells happens and repeats into new neurons and astrocytes. PNPs showed promising potential in boosting neuroprotection, which is studied by Gan and his associates. Surface-engineered PNPs of RVG29-loaded with microRNA (miR)-124 were designed by Gan and co-workers to improve neuroinflammation in PD. Polymeric NPs were prepared using a double-emulsion technique, and maleimide–thiol interaction was used for RVG29 conjugation onto the NP surface. In vitro drug release data demonstrate sustained miRNA release up to 60 h with approximately 40% of released in 24 h while ∼70% release at 60 h. RVG29-conjugated miRNA-NPs showed higher permeability in vitro BBB model in comparison to nontargeted NPs. MTT assay performed in BV 2 cells showed no toxicity of blank NPs for <100 μg/ml concentrations, indicating the safety of NPs. A marked decrease in cell viability after treatment with 200 μg/ml of placebo NPs was observed. Results reported a significant increment of inducible nitric oxide synthase (iNOS), tumor necrosis factor-alpha (TNF-α), cytokines (interleukin-6), and mRNA levels after lipopolysaccharide administration. However, the levels of mRNA in the miR-NP treated control group and the abovementioned cytokines were found almost equal, suggesting miR-124 exposure. Also, miR-NPs showed a significant reduction in expression of P-P65 and MEKK3 protein kinase. The studies indicated that miR-124 could target nuclear factor kappa B cell (NF-κb) pathways and MEKK3. mi-RNA-NPs results in the downregulation of MEKK3 expression in animal studies with ca. threefold decrease in cell apoptosis. The research revealed that mi-RNA-NP exhibits the potential to boost neuroprotection by inhibiting pro-inflammatory signaling (Gan et al., 2019).

Psychotic disorders are clinically driven by cognitive conditions, i.e., delirium, dementia, hallucination, delusions, and schizophrenia. Conventionally available antipsychotics suffer from poor bioavailability, significant extrapyramidal effects, poor brain delivery due to the BBB, and drug-related peripheral toxicity. PNPs are under clinical trials for the management of psychotic symptoms and emerge out as more efficient and efficacious for delivery of antipsychotics to the brain (Annu Rehman et al., 2019). A rational (ligand-based PNP) approach for targeting antipsychotic drugs to the brain to overcome the limitations of conventional dosage forms is under research and discussed below.

T80-coated chitosan NPs of doxycycline hydrochloride were prepared by Yadav and associates for the treatment of psychosis. Optimized NPs were evaluated for their efficacy in the ketamine-induced psychotic mouse model. The NPs exhibited 237-nm particle and 78.16% drug entrapment efficiency. The NPs easily passed through the BBB and demonstrated significant antipsychotic activity. A marked increase in GSH and GABA levels was observed after oral administration of T80-coated doxycycline hydrochloride NPs in ketamine-induced psychotic mice. However, a marked decrease in MDA level, TNF-α, and dopamine levels was noticed in the NP-treated group compared to the toxic group. The above results indicated the enhanced penetration of doxycycline hydrochloride through the BBB with T80-coated NPs (Yadav et al., 2017).

Author’s opinion: The study demonstrated the potential of targeted NPs for the management of psychotic disorders and might be potential carriers in the treatment of neurological disorders.

GBM is the most destructive and common kind of brain tumor, affecting a large number of populations globally. Chemotherapy for the treatment of brain tumors is a challenging therapy, and the presence of the BBB also hinders the permeation of active drugs to the brain. GBM treatment is the most difficult despite having multimodal treatment facilities like radiation therapy, systemic chemotherapy, and surgical incision (Li et al., 2014). Moreover, new diagnostic strategies such as immunotherapy, new drugs, and PNPs are currently the subject of clinical trials for GBM treatment. Ligand-conjugated PNPs have shown potentiality in the treatment of GBM due to specific drug delivery at the tumor site. Targeted PNPs designed by various researchers for brain tumors treatment are described below.

Malignant brain tumors often cause alteration or disruption of the BBB, which causes an increase in heterogeneous vascular permeability throughout the tumor and its outside (Sprowls et al., 2019). The vascular delivery of therapeutics in brain tumors is hindered by the characteristics of both the BBB and the blood–brain tumor barriers (BBTB). The transport of many therapeutics and fluorescent depends on the extent of vascular permeability, as many of them reach the tumor via vasculature, thus limiting the extent of treatment in the region of the tumor (Belykh et al., 2020). The disruption of the BBB is a key barrier to the treatment success of brain tumors (Karmur et al., 2020).

Chlorotoxin (Cltx)-consolidated-alisertib/silver-(Ag)-NPs were prepared via nanoprecipitation using PLGA-b-PEG-COOH as copolymer. In vitro studies conducted in 87 MG human glioblastoma cell line revealed that with increasing concentrations of alisertib (0.001–10 μM) in Cltx-consolidated-alisertib/Ag-NPs, the cell viability decreased when compared to control (untreated cells). The cell viability was found to be 98% and 99%, respectively, after 48 and 72 h of exposure to NPs as compared to alisertib alone at each time point. Figure 8 shows the comparative analysis of Ag PNPs and Cltx/alisertib-consolidated-Ag-NPs injected in tumor-bearing mice. Nontargeted Ag-NPs-^99mTc showed approximately 0.6% concentration in the tumor after 60 min of injection, indicating the enhanced retention and drug permeability. Also, Cltx consolidated alisertib/Ag NPs reduced the tumor growth size, revealing the synergistic effect as compared to Cltx consolidated Ag NPs and control groups, which did not show a marked effect on the size of the tumor. The above research concluded the potentiality of these novel therapeutics for targeted delivery of therapeutics in the treatment of GBM (Locatelli et al., 2014).

GSH-conjugated PEG-PLGA NPs of DTX were prepared to enhance the brain targeting efficiency of DTX in brain tumors. In vitro results indicated the burst release of DTX initially from NPs for 24 h following the controlled release of DTX (18.49% ± 5.21%) for 10 days. MTT assays in C6 and RG2 cells revealed that GSH-conjugated NPs of DTX reduce the cell viability when compared to untreated cells and PEG-PLGA NPs and DTX suspension. The permeation of the drug was analyzed utilizing in vitro BBB (Transwell™) model. GSH-conjugated PEG-PLGA NPs showed time-dependent release of DTX in the first 16 h followed by constant release over 48 h, suggesting the ability of NPs in permeating the BBB (Grover et al., 2014).

Author’s opinion: The above research concluded that GSH-conjugated PEG-PLGA NPs of DTX could be a novel approach in targeting DTX to the tumor site via the existing transport mechanism of GSH in battling the brain tumor.

Aptamer (U2)-conjugated gold NPs were prepared for GBM therapy. U2-gold NP complex was synthesized by dissolving 5ʹ thiol-modified aptamer in phosphate buffer and then deprotecting in dark with TCEP. Aptamer and TCEP were separated using the NAP-5 column, and then U2 was purified. Excess of gold NPs was added to purified U2 and underwent 20-min reaction; then 0.1 M of phosphate buffer and sodium chloride was added and kept overnight for a reaction and then centrifuged for 30 min to remove aptamer and free gold. Cell line studies in U87-EGFRvIII depicted that U2 aptamer-conjugated gold NPs cross the BBB and reach the tumor by inhibiting the EGFR pathway and helping in preventing damage DNA repair in cells of GBM. In vivo study conducted in GBM-bearing mice indicated prolongation in mice survival rate with U2-conjugated gold NPs as compared to normal saline-treated mice. The above findings suggested the potential of aptamer (U2)-gold NPs as a targeted drug carrier for GBM therapy (Peng et al., 2020). Table 1 summarizes the different kinds of PNPs used for drug-targeting to the brain tumor.

AD is a chronic and growing neurodegenerative disorder that occurs due to the accumulation and accretion of Beta-amyloid (βA) peptides (Querfurth and LaFerla, 2010). AD is a protein conformational disease that is primarily caused by soluble protein aberrant processing and polymerization (Tiwari et al., 2019). Conferring to the UN Aging Program and US Centers for Disease Control and Prevention, it has been predicted that there will be an immense increment in the populations (above the age of 60 years) from 420 million to 1 billion by 2030 (Qiu et al., 2009; Trends, 2003; United Nations (2002). De, 2002). Moreover, the availability of present treatments is unable to cure or delay the advancement of AD, as most drugs are unable to permeate through the BBB and thus unable to reach the brain target site (Xu et al., 2020). Therefore, there becomes a need to develop NPs by incorporating the drugs to improve the targetability and therapeutic efficiency of AD drugs.

Rhynchophylline (RIN) is the main active tetracyclic oxindole alkaloid stem found to be effective in the treatment of AD, but its poor aqueous solubility, penetrability, and bioavailability limit its use in AD. Therefore, to achieve its therapeutic effect, Xu and his associates developed methoxy PEG-PLGA NP loaded with (RIN) attached with T80 (T80-NPs-RIN) using the nanoprecipitation method to enhance its brain targeting efficacy. In vitro BBB study was carried out among NPs and T80-NPs-RIN using mouse brain endothelial cell b.End.3, and it was observed that the uptake efficiency of T80-NPs-RIN in b.End.3 was higher when compared to that of uncoated NPs. Moreover, the incorporation of T80 in the formulation resulted in improvement in the neuroprotective outcome. Additionally, the hemolytic data revealed that T80-NPs-RIN did not instigate any hemolysis, displaying virtuous biocompatibility. Hence, the study was later concluded by depicting that the T80-coated NP had more efficiency towards the treatment of AD therapy as compared to NPs and free RIN (Xu et al., 2020).

Fan et al. developed an innovative brain targeting PLGA-PEG NPs loaded with curcumin (CUR) attached with B6 peptide using the ring-opening method. HT22 cells were used to perform cellular uptake study and cytotoxicity studies among the developed formulations (PLGA-PEG-B6/CUR), free CUR, uncoated formulation (PLGA-PEG/CUR), and PLGA-PEG-B6 NPs. It was observed that all the particles were compatible and exhibited a low toxicity profile as shown in Figure 9A. On the other hand, in the case of the cellular uptake study, it was observed that PLGA-PEG-B6/CUR NPs enormously enhanced their cellular uptake when compared with other formulations. The uptake effectiveness was found to be enhanced from 8.94% ± 1.10% to 45.72% ± 0.48% as shown in Figures 9B–D. Morris’s water maze parameter further demonstrated that PLGA-PEG-B6/CUR could immensely upsurge learning and memory capacity on APP/PS1 mice when compared with free CUR. Moreover, the data obtained by performing ex vivo parameters, for instance, immunostaining, Western blotting, and Bielschowsky’s silver staining displayed that PLGA-PEG-B6/CUR could inhibit the hippocampal βA development followed by deposition of tau-hyperphosphorylation. Therefore, it was concluded that PLGA-PEG-B6/CUR is a more promising carrier for the management of AD (Fan et al., 2018).

As per the etiology of AD, deteriorated interaction between βA with a surplus quantity of metal ions is found (Castellani et al., 2010). Thus, surpassing this disruption via NPs can be a better approach. Therefore, Sun et al. developed quercetin-loaded PLGA NPs (PLGA at Q) NPs via the double emulsion solvent evaporation technique. The developed formulation showed less cytotoxicity on SH-SY5Y cell lines in addition to inhibition and disruption assay on Aβ₄₂ fibrils depicting that PLGA (at Q) NPs had more potential than any other formulation. It was further observed that there was a dose-dependent effect of the formulation on SH-SY5Y cells. Moreover, it was observed that the developed formulation had the potential to obstruct the neurotoxicity of Zn²⁺–Aβ₄₂ and further increase the feasibility of neuron cells. The data obtained by performing behavioral studies using APP/PS1 mice depicted that the formulation was able to limit cognition and memory damage. No adverse effects of the formulation were reported in any of the organs after the histopathological study. Thus, the study was then concluded by stating that the prepared nanoformulation was efficient in delivering the drug at the targeted site with increased therapeutic efficacy and decreased side effects (Sun et al., 2016). Table 2 depicts the PNPs used for drug-targeting to the brain for the treatment of AD.

Stroke is a clinical condition that comprises the development of disturbance in the focal signs of cerebral functions lasting for more than 24 h or causing the demise of the patient with no deceptive cause apart from those having vascular origin (Chugh, 2019). Stroke has been categorized depending upon the hurdle in the supply of blood through the blood vessels to the brain, which includes hemorrhagic stroke and ischemic stroke. Hemorrhagic stroke arises due to the falling out of blood out of the blood vessels leading to the spilling of blood in the intracranial cavity, whereas ischemic stroke happens due to the obstruction of the blood vessels that restricts the blood supply to the brain (Musuka et al., 2015). Besides, ischemic stroke covers 68% of all strokes globally than hemorrhagic stroke accounts for 32% (Lozano et al., 2012). Thus, there becomes a necessity to develop a nifty drug delivery system with the required biological and physicochemical properties including targeting ability, extended circulation time, and sustained release of drug to specific target cells.

Ischemic stroke is associated with the enhancement in reactive oxygen species (ROS) in the ischemic neuron causing the injury or death of the neurons. So Lv and associates formulated a ROS-sensitive nanocarrier to deliver the neuroprotective agent, i.e., NR2B9C at the stroke site in contrast to ischemic brain damage. The nanocarrier is comprised of a dextran polymer core altered with the boronic ester (ROS-sensitive) along with a red blood cell (RBC) membrane shell followed by insertion of the homing peptide (SHp). The developed NP (SHp-RBC-NP) showed controlled release of NR2B9C at ischemic brain tissues. Additionally, the study further revealed that the formulation possessed marked cytotoxic activity against glutamate-induced cytotoxicity in PC-12 cells. Moreover, the data obtained by performing in vitro and pharmacokinetics studies showed that NPs could considerably extend the systemic circulation of NR2B9C, thereby targeting the ischemic brain tissues. Therefore, the study was concluded by suggesting that the developed nanocarrier could produce effective treatment against ischemic brain damage (Lv et al., 2018).

Han and associates designed chlorotoxin (CTX)-modified PLGA NPs of Lexiscan (Lx) to improve the BBB permeability of Lx and autocatalytically augmenting stroke-targeting delivery of NPs to the ischemic microenvironment into the brain. The CTX-modified Lx NPs specifically accumulated to the ischemic brain microenvironment compared to unmodified NPs, and an increment in targeting efficiency was observed. The above findings reveal that CTX can be a promising ligand for targeted delivery of therapeutics to the ischemic brain region. The targeted delivery of NPs using CTX as a ligand could be a new approach for better management of stroke (Han et al., 2016).

Researches revealed that by the use of proangiogenic genes, ischemic stroke prognosis can be improved by improving angiogenesis at the site of injury. So hypoxia-inducible factor 1-α (HIF-1α), which has an angiogenic effect, was encapsulated to hyperbranched cationic amylopectin derivative (DMAPA-Amyp) NPs and modified with RGD peptide for directly delivering it to the endothelial cells of the brain peri-infarct site. Findings suggested higher cell uptake and good biocompatibility of RGD-DMAPA-Amyp, indicating the endocytosis of this nonviral gene vector by human cells and its safety. Studies conducted in ischemic stroke rat models demonstrated higher aggregation of RGD-DMAPA-Amyp NPs to the brain pre-infarct region and vascular endothelial cells with significant enhancement in neurological function recovery. In vivo results indicated significant promotion in new blood vessel formation by RGD-DMAPA-Amyp/HIF-1α-AA. The results indicated that RGD-modified NPs are the safe and promising therapeutic strategy for delivering non-viral gene vectors to the brain for ischemic stroke therapy (Deng et al., 2019).