*Corresponding Author:
A. Anita Margret
Department of Biotechnology and Bioinformatics, Bishop Heber College
E-mail: [email protected]
Date of Submission 15 October 2015
Date of Revision 19 October 2016
Date of Acceptance 18 February 2017
Indian J Pharm Sci 2017;79(2):186-196  

Abstract

Biopolymer such as chitosan is more favoured as a drug carrier in particular to the brain due to its potential to cross the blood brain barrier. This study is a comparative assessment of the extraction of chitosan from natural sources such as mushroom, crab and shrimp using alkali method pursued by physicochemical assays that surmise the excellence of the biopolymer in permeating a central nervous system drug. Commercially, chitosan extracted from crustaceans have been widely used but this study revealed that mushrooms are also a good source for chitosan. An in silico assay enumerates the structural affiliation of the polymer and its binding efficiency. Molecular docking study facilitates to attest the brain targeting efficiency of chitosan on disparity with sodium alginate against the efflux permeability glycoprotein furnishing a minimum binding affinity energy values of -37.2 kcal/mol. The pharmacologically significant descriptors propose a low solubility that avoids the untargeted discharge of drug. Chitosan extracted from a rich protein source such as mushroom in a mild alkaline condition with a high degree of deacetylation has freer amine groups can act as a drug by itself and can readily bind with a drug as a carrier. The synchronised work of biopolymer extraction with that of in silico analysis can further take chitosan as a lead compound for brain drug development and targeting studies.

Keywords

Biopolymer, chitosan, central nervous system, molecular docking, blood brain barrier, permeability, glycoprotein

Polymers partake a vital role in drug delivery system as they control the release of the drug from a delivery system. Natural polymers promote drug delivery due to their physicochemical characteristics, ease of availability, biodegradable nature and lack of appreciable toxicity. Hence, biopolymers exhibit the potential to enhance medical treatment by minimizing adverse effects. Biopolymers are polymers produced by living organisms and chitosan is a natural polymer obtained by deacetylation of chitin. Further it has better stability and versatility of being applicable to various routes of drug administration [1]. The deacetylated chitosan consists of glucosamine units as the backbone, which has a high density of charged amine groups, permitting strong electrostatic interactions with proteins and genes that carry an overall negative charge at neutral pH [2]. The physicochemical properties of chitosan play a significant role in drug delivery that has been illustrated quite elaborately in the literature [3]. Commercial chitosan is extracted from crustaceans, but is subjected to harsh chemical treatments. Chitosan is produced from shrimp and crab shell chitin by deacetylation using strong alkalis at high temperatures for long periods of time [4]. However, supplies of raw materials have been variable with season due to the laborious and costly process. Furthermore, chitosan derived from such a process is heterogeneous with respect to physiochemical properties [5]. Considering these aspects there is a necessity to perform a comparative study of the extraction and characterization of chitosan from all three bio resources such as crab, shrimp and mushroom using a mild alkaline method. Moreover, chitosan extracted from mushroom was found to be on par with that extracted from crustaceans and could be used for various medical applications [6]. On the large scale, high amounts of chitosan is extracted from crustaceans, but advances in fermentation technology render the cultivation of selected mushrooms an alternative source of chitosan [7].

Polymers exhibit a good potential for surface modification by chemical transformations, which increases the solubility index [8]. This remarkable potential of biodegradable polymers is to provide greater pharmacokinetic control, which makes them suitable for entrapment and delivery of a wide range of therapeutic agents [9]. Chitosan has the potential of serving as an absorption enhancer across epithelial membranes due to its mucoadhesive and absorption enhancement properties. This distinguished feature of chitosan is likely to enhance the drug dispersion in the gastrointestinal tract that ultimately improves bioavailability of various drugs. Drugs targeting central nervous system (CNS) must cross the blood brain barrier (BBB), which is the main obstacle for a variety of molecules to enter the CNS tissue [10]. The use of biocompatible nanoparticles to facilitate the traverse of drugs across BBB has been extensively researched in the past decade [11]. In drug delivery, selection of an ideal type of biopolymer like chitosan might result in sustaining drug delivery to prolong the duration of action, improve therapeutic efficiency and simultaneously reduce side effects. Chitosan might as well aid in brain drug targeting by being an ideal carrier for drugs through the BBB. The present study aimed at developing an alternate bio resource to produce chitosan with a comparative physicochemical profile. The present investigation also employed docking analysis to investigate the brain targeting capability of the biopolymer.

Materials and Methods

All chemicals used were of the highest available commercial grade. Commercial chitosan from shrimp shells (≥85% deacetylated) was purchased from HiMedia Laboratories (Mumbai, India) and other chemicals such as sodium hydroxide, hydrochloric acid, ethylenediaminetetraacetic acid (EDTA) and bleaching powder were obtained from Scientific Research Laboratory Ltd (Chennai, India).

Collection of samples

Commercially available freshly packed edible mushrooms were purchased from super market store. The mushroom species was authenticated as Agaricus bisporus (No. AA 001) in the Rapinat Herbarium and Centre for Molecular Systematic, St. Joseph’s College Tiruchirappalli, Tamil Nadu, India. The exoskeleton of crab and prawn was collected from the central market of Tiruchirappalli, Tamil Nadu, India.

Extraction of chitosan

The purchased mushroom (A. bisporus) samples were washed exhaustively with water after adjusting pH with KOH to 8-9. Chitosan was extracted from the washed mushrooms with KOH and HCl using a method developed by combination and modification of protocols implied earlier [12,13]. Mushroom biomass was treated with 60% (w/v) aqueous KOH solution (10 ml per 1 g of dry mycelium) at 130° for 2-3 h to remove proteins, lipids and alkali-soluble polysaccharides. For chitosan isolation, this freeze-dried alkali insoluble fraction was boiled with 0.1-1% (v/v) acetic acid solutions (50 ml per 1 g of dry matter) for 10-40 min. The pH value of the acidic supernatant was increased to 9.5 with 2 M NaOH. The alkali-insoluble precipitate (presumable chitosan) obtained was repeatedly centrifuged and washed with distilled water, freeze dried and weighed.

The shells of crab and prawn were washed, dried and powdered. The powdered exoskeletons were suspended in boiling NaOH (2 and 4% w/v) for 1 h, which facilitated the isolation of crude chitosan by dissolving the proteins and sugars. The samples were treated in two different concentrations of NaOH where, the higher concentration (4%) is used for chitin preparation [14,15]. Further at room temperature the shells were subjected to demineralization using 1% HCl where, the minerals (mainly calcium carbonate) are removed [16]. The demineralization process was preceded by treating the samples with 50 ml of a 2% NaOH solution to decompose the albumen into water soluble amino acids. The remaining chitin was washed and further converted into chitosan by the process of deacetylation [17], which was carried out by boiling the samples in 50% NaOH for 2 h on a hot plate. Repeated washing with 50% NaOH and filtration retained a solid matter, thus extracting chitosan as whitish flakes. The obtained chitosan was purified to increase its commercial value using three process such as filtration, reprecipitation and demineralisation [18]. The insoluble fraction of the sample was removed by filtration through Whatman filter paper 22 μm. Chitosan was precipitated from filtered chitosan solution by titration with 1 N NaOH until a pH value of 8.5 is attained. The chitosan so obtained was washed several times with distilled water by centrifuging at 8000 to 10 000×g. Demineralisation is the final process in the extraction of chitosan where, 1 ml of 10% w/v aqueous sodium dodecyl sulphate (SDS) was used for dissolving the remaining protein. The samples treated with SDS overnight were exposed with 3.3 ml of 5% w/v EDTA for complexing heavy metals with EDTA. Repeated centrifugation extracts the insoluble fractions and the residue obtained is dried and used for commercial purpose.

Characterization of prepared chitosan

A homogeneous mixture of 1 mg/ml (w/v) concentration of chitosan solution was prepared with 1% glacial acetic acid to analyse and characterise various parameters such as degree of deacetylation (DD), pH, ash value, loss on drying and assaying its functional group. DD referred to removal of acetyl group from the chain, which was determined by potentiometric titration [19]. DD% = 100−DA. The pH measurements of the chitosan solutions were carried out using a pH meter (Elico model no IL120). To determine the ash value of chitosan, samples were heated in a muffle furnace and the percentage of ash value was calculated using the following Eqn. [20], ash value (%) = weight of the residues (g)/weight of the sample (g)×100. Loss on drying of the prepared chitosan was determined by the gravimetric method of Black [21], the result of which was expressed as % loss on drying, which was (wet weight–dry weight)/dry weight×100.

Fourier transform infrared spectroscopy (FTIR) spectroscopy of solid samples of the extracted chitosan was done on a Bio-Rad FTIS-40 Model USA. Ten grams of sample was mixed with 100 g of dried potassium bromide (KBr) and compressed to prepare a salt disc (10 mm diameter) for reading the spectrum further. The FTIR profile of the standard chitosan was analysed using a FTIR spectrum.

Preparation of chitosan

The original ligand structures of the target was drawn and prepared (Figure 1a-c). The structures of the chitosan (CID: 71853), sodium alginate (CID: 6850754) and chitosan oligosaccharide lactate (CID: 16213812) were downloaded from Pubchem. The H bonds were fixed and the energy minimized structures were generated using ACD/ChemSketch ACD (2009).

Pharmaceutical-Sciences-target-protein

Figure 1: Structures of the biopolymers as ligands and target protein
a. Chitosan (CID No: 71853); b. sodium alginate (CID No: 6850754); c. chitosan oligosaccharide lactate (CID No: 16213812); d. crystal structure of P-gp (PDB No: 4M1M)

Docking of the chitosan and hits with the target

The ligand compounds folder was loaded. Population size was set to 200. Number of generations was set to 25 and 2 best poses were retrieved. From the output folder, the binding energy for the best pose of the ligand was noted. The hydrogen bond interaction between the ligand and the binding site residues were analysed and interaction table was created and saved. The best compounds were identified based on the energy values and the fitness score was calculated based on the total energy of a predicted pose in the binding site.

Absorption, distribution, metabolism, and excretion-toxicity (ADMET) property prediction and molecular docking studies

Molecular docking evaluates the interaction of chitosan and the targeted protein permeability glycoprotein (P-gp) using Hex 8.0.0 software. The study also incorporated the drug delivery related properties of chitosan by structural activity relationship using Medchem Designer version 3.0. The target protein, P-gp was downloaded from Protein Data Bank (PDB ID 4M1M, Figure 1d). The structures were visualized using the molecular graphics program PyMol intended for the structural visualization of proteins, nucleic acids and small biomolecules and then loaded into Hex. The binding site was specified exactly based on the ligand group. The distance of the binding site was set to 8 Å.

Results and Discussion

Crude chitosan was extracted from all three bio resources, mushroom, crab and prawn (Figure 2a, b and c) with the removal of proteins followed by demineralization, which included the eradication of carbon and other salts proceeded by the deacetylation of the chitin. The extracted product was creamy white in colour with a crumble texture. When subjected to light the sharp edged flakes glittered. The percent biomass, in the production of crude chitosan was found to be, crab 5.8 g, (17.46 %), prawn 5.2 g, (15.65%) and mushroom 4.6 g (13.85%). The pH analysis of the extracted sample ensured alkalinity at 8.5.

Pharmaceutical-Sciences-chitosan-extracted

Figure 2: Chitosan extracted from various bio sources
Bio source and the appearance of chitosan extracted from those. Chitosan from a. mushroom; b. crab; c. prawn

The loss of water content from chitosan extracted from mushroom, crab, prawn and standard (commercial sample) was evaluated. All the three bio resources elected as test samples are moist with a constant and equivalent moisture content. But, the extracted chitosan from these test samples exhibited distinctive values that differ from each other. Eventually the moisture value of commercial chitosan is <10% [22] and Figure 3a represented a bar graph illustration, where the moisture value of crab chitosan is in close proximity to the standard chitosan. Polymers like chitosan were semi crystalline (partially crystalline amorphous) in nature hence it would be difficult to interpret the structure if the moisture content is high. Crystals are commonly nano-scaled in size and self-assembled nanostructures were proved to be highly effective in drug delivery [23]. Hence, chitosan should be dry and as per the data received compared to the standard, the extracted biopolymer from crustaceans has a high percent loss on drying as compared to that from mushroom. This may be due to their habitat and influence of salinity. The ash content from the extracted chitosan of all three bio resources was compared with that of the standard. As evaluated with the commercial sample meagre differences were found in the chitosan extracted from crab and mushroom. The ash values are analogous to each other (Figure 3b), which could be interpreted as due mainly to the inorganic content present in the biopolymer. Minerals are elements that aid in structure formation partaking as components of biologically active molecules with beneficial effects [24]. The luminal membrane of the brain endothelium (facing blood capillary) is lined with ATP binding cassette family of active efflux transporter pumps like P-gp, multidrug resistance protein (MRP) and on the abluminal surface of choroid plexus is the multi specific organic anion transporter (MOAT) [25,26]. They act as a restraint to remove the un-intended drugs/substances (lipophilic/ neurotoxic) from the endothelia cell cytoplasm, before it could cross the brain parenchyma [27] hence, there is a need of a carrier, which can pass through this efflux protein. Chitosan has an adhesion property that plays an important role in the interaction of its positively charged amino group with the negatively charged sites on the epithelial surface. It has been reported that chitosan can adhere to the mucosal surface and transiently open the tight junctions between epithelial cells, thus it’s an effective absorption enhancer. There is a need of energy-dependent process and divalent cations such as Ca2+ to regulate the tight junction permeability [28]. Therefore the presence of inorganic contents and minerals benefits chitosan as a carrier into the BBB and mushroom expedites as a bio resource with a characteristic ash value.

Pharmaceutical-Sciences-commercial-sample

Figure 3: Comparative analyses of extracted chitosan with commercial sample
a. Loss on drying; b. ash value; c. degree of deacetylation

The DD of the extracted chitosan from crab, prawn and mushroom was assayed by means of potentiometric titration along with the standard chitosan. DD is one of the main parameters characterizing chitosan. The calculated values are depicted with a graphical representation (Figure 3c). The extracted chitosan from all three resources comprised of DD value of ≥75, which confirmed that chitin is deacetylated and it becomes soluble in the acid. The process of deacetylation involves the removal of acetyl groups from the molecular chain of chitin, leaving behind the biopolymer (chitosan) with a high degree chemically reactive amino groups (–NH2). This makes the DD an important property in chitosan production as it has a significant role in endorsing physicochemical characterisation thereby enhancing drug delivery [29]. A polymer with a high deacetylation value supplements the required protein constitution that reduces immunogenicity and limits the phagocytosis of drug by the reticuloendothelial system. This results in an increased drug concentration in blood and vital organs such as the brain, intestines and kidneys [30].

Chitosan is a cationic polymer that has the capacity to chemically bind with negatively charged macromolecules. Hence, chitosan have attained increasing commercial interest as suitable resource materials due to its biocompatibility, biodegradability, adsorption properties that facilitate into epithelial cells. The crystallinity of the chitosan increases with the increase in DD and is attributed to increase in intermolecular hydrogen bonding due to the presence of more free NH2 groups (higher DD) within the molecular structure, which in turn results the better packing of the macromolecular polymeric chains and consequent increase in the crystallinity [31]. Crystals in nanoscale has the enhancement of penetration into biological membranes, hence a polymer like chitosan with a good DD can act as an incredible brain drug carrier to penetrate into the BBB.

The FTIR study allowed the comparison of the functional groups in all the three samples extracted from different bio sources with the standard. Figure 4a, b, c and d illustrated the spectral details of the extracted chitosan from three bio resources, crab (S1), prawn (S2) and mushroom (S3) besides the standard chitosan (S) and Table 1 listed the FTIR peak assignments of all the four samples. In order to characterize the test samples, spectrum of standard chitosan (S) is recorded with distinctive peaks having major absorption band at 3435 cm-1due to stretching vibrations of OH groups. Relatively the chitosan sample extracted from S2 and S3 had the same groups at 3465 cm-1 and 3423 cm-1. Whereas the spectral profile of S1 had a discrete band at 3233 cm-1 owing to the NH2 stretching vibration. Asymmetric stretching vibrations of C–H bond in – CH2 and –CH3 attributed to the pyranose ring at 2922 cm-1, 2862 cm-1 featured in the spectrum of standard chitosan (S), where the C–H bond in –CH2 pyranose ring is identical in all the three samples S1 (2913 cm- 1), S2 (2931 cm-1) and S3 (2926 cm-1). Absorption at the range of 1649 cm-1, S corresponds to the vibrations of carbonyl bonds –C=O in acetamide group (amide I band). This functional groups closely relates itself to the biopolymer and similar spectral peaks were found in S2 (1612 cm-1) and S3 (1647 cm-1). The bending vibrations of spectral peaks of S1 (1595 cm-1) and S3 (1570 cm-1) are associates with the protonated amine group. Bending vibrations of methylene and methyl groups were evident at 1379 and 1427 cm-1 in the standard sample [32]. Respectively, all the three samples have the presence of bending vibrations δ (C-H) at S1 (1421 cm-1), S2 (1415 cm-1), S3 (1417 cm-1) and 1380 and 1321 cm-1 at S1 and S2. Absorption in the range from 1160 to 1000 cm-1 has been attributed to vibrations of CO group [33]. The band located at 1153 cm-1 in S and S1 is related to asymmetric vibrations of in the oxygen bridge resulting from deacetylation of chitosan. The bands near to 1095-1025 cm-1 are attributed to the stretching vibrations of C–O in the ring of COH, COC and CH2OH, which is uniformly found in all three test samples and standard. The extracted chitosan was authenticated with the standard biopolymer using FTIR studies. All the three extracted samples have similar functional groups there by characterizing itself as chitosan.

Pharmaceutical-Sciences-spectra-chitosan

Figure 4: The FTIR spectra of chitosan
a. Standard-S; b. crab-S1; c. prawn-S2; d. mushroom-S3

Vibration mode* Standard chitosan Crab Prawn Mushroom
ν s( C-O) 1030 1027 1028 1035
  - 1082 1093 1074
ν as(C-O-C) 1153 1153 1126 -
ν (C-O) 1255 1260 - -
δ (C-H) 1379 1380 1321 -
  1427 1421 1415 1417
(-C=O) (amide I band) 1649 - 1612 1647
δ(NH) - 1595 - 1570
ν as(C-H) 2922 2913 2931 2926
ν (NH) - 3233 - -
ν (O-H) 3435 - 3439 3423

Table 1: Wavelength of the main bands obtained for the standard chitosan and chitosan extracted from mushroom, crab and prawn

Molecular docking and ADMET predictions are two imperative in silico techniques used to unveil the pharmaceutical significance of chitosan. The binding efficiency of the biopolymer was evaluated against the efflux protein P-gp and tabulated in Table 2. The binding site of the target was prepared and the energy minimized compounds were imported. Docking studies are devised for virtual screening to analyse the potential of the compound acting as a drug. This works deals with the study of analysing the efficiency of chitosan as a potential drug as a carrier transient through the BBB. The permeability glycoprotein or plasma glycoprotein is an active, efflux, membrane bound transport protein pump [34]. Though chitosan has established itself as an efficient drug carrier, its high molecular weight intervene the interaction between the proteins. Hence, chitosan derivative such as chitosan oligosaccaharide lactate is incorporated as drug delivery system while encapsulating ocular drugs [35].

Ligand Affinity (kcal/mol)
Chitosan –27.4
Chitosan oligosaccharide lactate –23.18
Sodium alginate –37.2

Table 2: Binding affinity value by molecular docking against P-Gp

Based on the experimental study, chitosan is docked against P-gp through in silico rigid docking approach where the ligand is flexible and protein is static. The docking results showed that both the ligands (chitosan and its derivative) interacted with the target protein (P-gp surrounded by several donor atoms of chitosan residue) on the surface with a free binding energy of –27.4 and –23.18 kcal/mol (Figure 5a and b) whereas, sodium alginate (reference polymer) interacted with a minimum affinity value of –37.2 kcal/mol. Though the minimum energy score of chitosan oligosaccharide lactate was greater than sodium alginate, it exhibited interaction with the protein through the residues PHE 974, PHE 724 (Figure 5c and d). Interestingly, these residues also responded with the bioactive co crystallized ligand flavin-adenine dinucleotide (FAD) and antidepressant drug, venlafaxine [36]. The docking simulation studies of chitosan deduce PHE 974, PHE 724 as interacting key residues, which also found in the standard antidepressant drug venlafaxine and ligand FAD. The molecular modelling showed the participation of biopolymer with the protein by means of H–OH interaction. Hence, the biopolymer has the prospective of inhibiting the efflux protein P-gp, thereby facilitating the drug through the BBB.

Pharmaceutical-Sciences-drug-polymers

Figure 5: Best docked conformations of drug polymers
a. Chitosan with the protein P-gp; b. chitosan oligosaccharide lactate with the protein P-gp; c. interaction of the ligand chitosan oligosaccharide lactate (red) within the active site residues of the target; d. sodium alginate with the protein P-gp

An idyllic drug carrier releases the drug precisely under the varying environmental stimuli. Computational studies like structure activity relationship (SAR) aids in designing a smart delivery system, which is prudent and efficient. In concern to this, a preliminary study has undergone highlighting the pharmacologically significant descriptors. Some calculated structure activity values (log P, log D, topological polar surface area and Hydrogen bond donor and acceptor protons) of the biopolymers correlates to the ADMET properties of a drug. Table 3 represented the values of all three-test polymers. Aqueous solubility is one prime pharmacological property of a drug carrier and some have low solubility values [37]. A drug carrier with a high solubility index has the chance to disintegrate thereby dispersing the drug before it could reach the target, which influences the bioavailability of the encapsulated drug [38].

Drug carriers log P log D Topological polar surface area HBDH No of H2 bond donor protons M_NO No ofN2and O2atoms
Chitosan -12.000 –13.945 5808.00 37.00 48 .00
Chitosan oligosaccharide lactate -3.264 -4.00 6201.11 11.00 10.0
Sodium alginate -5.208 -5.208 320.14 16.00 19.00

Table 3: Some of the calculated admet descriptors as drug carriers

Hence, drug carriers with low solubility value are constant leading in the definite distribution of drugs to the targeted sites. Partition-coefficient (P) or distribution-coefficient (D) is the proportion of a drug in a mixture of two immiscible phases, which is the indicator of solubility. Log P value is the measure of lipophilicity of a compound that assesses its dispersion in a medium [39]. The physiochemical descriptors illustrate a low log P value for chitosan (–12.000) when compared to chitosan oligosaccharide lactate (–3.264) and sodium alginate (–5.208). Hence, the dispersion rate of chitosan is more in aqueous medium and prevents the disintegration of the drug from reaching the target. The dissociation factor of a drug carrier influences the distribution coefficient value of drug even at varied physiological condition. Deviation in pH is due to the persistence of abnormal physiological condition and a drug carrier should be able to resist and continue stable. Log D value (Table 3) indicates the dissociation at the specified pH 7.4 where, chitosan dissociates low (–13.945) and prolongs to be so in the acidic conditions. It then gradually increases in the basic condition and this was similar in the log D values of chitosan oligosaccharide lactate (–4.283), which eventually increased in the basic conditions. But sodium alginate did not confer any disparity in the log D value between the acidic and basic conditions and among the acidic state –5.028 persist to be the unvarying.

Lipinski's rule attests the ability of a drug by devising rules that an ideal drug should not violate all the four rules. As mentioned earlier in the study high molecular weight of chitosan dissuades the drug likeness parameter whereas, chitosan oligosaccharide regulates this by persuading 3 rules of Lipinski (Table 4). Hence, the study elucidates chitosan as a drug carrier with more biocompatibility surpassing the BBB.

Drug carriers
weight
donor
Molecular
bond
acceptor
Hydrogen
bond
Hydrogen log P
Chitosan 1526.49 37.00 48 .00 –12.000
Chitosan
Oligosaccharide
Lactate
340.332 11.00 10.00 –3.264
Sodium Alginate 554.459 16.00 19.00 –5.208

Table 4: Calculated properties of lipinski’s rules for the drug delivery systems

The present study evidently unveils the significance of chitosan acting as suitable brain drug carrier. All though the extraction of this biopolymer from natural resources like crab, prawn and mushroom has been pioneered and customized commercially, this study attempts to axis the brain drug delivery to a distinct facet. On a large scale, chitosan is preferred to be extracted from crustaceans but, edible mushrooms like A. bisporus also has the potential to confer and this has been attested with an appreciable physicochemical characterization. The extraction of chitosan from mushroom was at ease, which also gave satisfactory results on par with the other bio resources and the method of extraction is malleable, when compared to the harsh chemical treatments. High DD and ash value infers the quality and drug binding mechanism of the polymer. These characterizations were performed to associate with the brain drug facilitation across the BBB. The docking stimulus interactions of chitosan and the targeted protein P-gp further substantiate the plausibility in facilitating brain drug across the epithelial barrier. As drug carriers the biopolymers should possess the capability of controlled drug release and the structural activity relationship studies paves way to determine the significant descriptors. The comparison of the predicted properties such as log P and log D were comparatively less. A low solubility in concert with a customary pH averts the adverse dispersal of drugs to the untargeted sites. Being a natural polymer chitosan and its derivatives are advantageous over other drug carriers. Application of nano science can assist the biopolymer coated drugs in reducing and avoiding adverse effects, thereby minimizing the duration of treatment. Neurological diseases are a threat to standard living and drug loaded with the extracted chitosan as would be an excellent remedy and can improve the quality of therapeutic value.

Acknowledgments

The authors acknowledge the support offered by the management of Bishop Heber and Jamal Mohamedh College, Tiruchirappalli, Tamil Nadu, India. Facilities provided by the Laboratory of DNA Bar coding and Marine Genomics, Department of Marine Science Bharathidasan University, Tiruchirappalli, Tamil Nadu, India are gratefully acknowledged. The authors also thank Dr. S. John Britto, Director, Rapinat Herbarium and Centre for Molecular Systematic, St. Joseph’s College Tiruchirappalli, for his assistance in authenticating the mushroom species.

Conflict of interest

The authors declare no conflicts of interest.

Financial support and sponsorship

Nil.

References