Research Article

Burned Wound Healing Effect of Prepared Pumpkin Seed Oil Nano Phytosome Loaded Lidocaine in Rabbit

Wafa’a Mohammad Abduwhab1*, Waseem Ali Hasan2, Mohanad Abdulsataar AL-Bayati3*

1Department of Physiology, Biochemistry, Toxicology and Pharmacology, College of Veterinary Medicine, Tikrit University, Iraq; 2Department of Physiology, Biochemistry, Toxicology and Pharmacology, College of Veterinary Medicine, Tikrit University, Iraq; 3Department of Physiology, Biochemistry and Pharmacology, College of Veterinary Medicine, College of Veterinary Medicine, University of Baghdad, Iraq.

Received | June 24, 2023; Accepted | July 20, 2023; Published | February 26, 2024

*Correspondence | Wafa’a Mohammad Abdulwahab, Mohanad Abdulsataar AL-Bayati, College of Veterinary Medicine, Tikrit University, Iraq; College of Veterinary Medicine, University of Baghdad, Iraq; Email: wafaadr619@gmail.com

Citation | Abduwhab WM, Hasan WA, Al-Bayati MA (2024). Burned wound healing effect of prepared pumpkin seed oil nano phytosome loaded lidocaine in rabbit. Adv. Anim. Vet. Sci. 12(4): 723-731.

DOI | https://dx.doi.org/10.17582/journal.aavs/2024/12.4.723.731

ISSN (Online) | 2307-8316

Copyright: 2024 by the authors. Licensee ResearchersLinks Ltd, England, UK.

This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

INTRODUCTION

The pumpkin plant originated in northern Mexico, Argentina, and Chile and has been spread to Western America, Europe, and Asia (Hancock, 2023). It known as “Kraa”, belongs to the family Cucurbitaceae (Prommaban et al., 2021). Pumpkin seeds, recognized as functional food by-products, contain a range of biologically active components, including flavonoids, phenolics, carotenoids, fatty acids, tocopherol, as well as vitamins like E and minerals (Hussain et al., 2021).

Nanotechnology is the use of science to enhance the effectiveness of medicine, with applications across biology, physics, chemistry, biotechnology, pharmaceuticals, and engineering. Nano, meaning “dwarf” in Greek, involves particles ranging from 1 to 100 nm in size (Demir, 2020; Hasan and Raheem, 2021). Phytosome, an advanced drug delivery system, is an evolved form of liposome particles and herbal formulation, it comprises phytoconstituents from plant extracts enclosed by a lipid layer (Mahmoudabad et al., 2023; Eftekhari et al., 2023). This system heightens the bioavailability of water-soluble phytoconstituents by enveloping them with phospholipids, leading to improved absorption in the intestinal lumen through simple diffusion. Consequently, it extends the drug’s action duration and enhances its delivery to target tissues (Yadav et al., 2010; Pawar and Bhangale, 2015). Phytosome formulation reduces herb extract toxicity; it counteracts the side effects of high-concentration herbs with equivalent amounts of phytosomes carrying the same extract. This reduces first-pass metabolism, resulting in decreased drug clearance and an extended half-life (t1/2) (Ghanbarzadeh et al., 2016; Singh et al., 2018). Burns, a severe form of trauma, can be caused by various sources, approximately 80% of burns stem from heat sources like hot liquids, solids, or fire, they are categorized into four degrees based on severity and depth: first-degree, second-degree, third-degree, and fourth-degree burns (Jeschke et al., 2020b). This present study aimed to transform pumpkin seed oil into a nanotechnology-based composition with encapsulated Lidocaine to enhance stability and therapeutic properties while minimizing side effects, and improving physical stability and enhanced entrapment efficiency. As well as evaluating the therapeutic efficacy of Nano phytosome pumpkin-lidocaine gel for healing third-degree burns.

MATERIALS AND METHODS

Experimental Animals

10 to 18-week- old ,white male and female adult rabbits weighting 2.5-3 kg the rabbit were given two weeks to adapt during which they were provided ad libitum access to food and water.

Institutional Animal Care And Use Committee (Iacuc)

Prior to conducting any experiment, the methodology and protocols used in this research were reviewed and endorsed in accordance with animal welfare ethical measurements by the Scientific Committee of the Department of Physiology, Biochemistry, Pharmacology, and Toxicology, College of Veterinary Medicine, University of Tikrit, and the Ethics Committee of the College of Veterinary Medicine, University of Tikrit, Salah Aldin– Iraq (IACUC#:.1285-18-7).

Animal Grouping

Twenty-five rabbits divided into 5 groups (n=5); each group treated separately as following:

First group: negative control rabbits leave without treatment. Second group: positive control rabbits treated with empty liposome. Third group: rabbits treated with ordinary pumpkin seed oil. Fourth group: rabbits treated with Nano phytosome pumpkin-lidocaine 100% gel. Fifth group: rabbits treated with Nano phytosome pumpkin 100% gel.

Preparation Of Nano Phytosome Pumpkin Seed

Cholesterol 0.5g, phosphatide choline 0.5g dissolved in mixed organic solvent chloroform 15 ml, methanol. The mixture was vortexed with a vacuum for 15 minutes, then incubated in a water bath at 40 ᵒC; the mixture was vortex and vacuumed for 20 minutes (Ghanbarzadeh et al., 2016). The blank liposome was created and then incubated in a water bath at 40 ᵒC for 5 minutes, 1 ml of pumpkin seed oil was mixed and vortexed for 2 hours, then removing the supernatant, the phytosome was formed (Lu et al., 2019).

Nano Phytosome Pumpkin Seed Encapsulated Lidocaine

The Nano phytosome pumpkin seed was incubated in a water bath at 40 ᵒC for 15 minutes. Lidocaine 0.5ml (0.2%) was added to pumpkin seed Nano phytosome 1 gm, then vortex for 1 hour, remove the supernatant, pumpkin seed Nano phytosome encapsulated Lidocaine was formed (Franz-Montan et al., 2015).

Entrapment Efficiency Procedure

The entrapment efficiency of Nano phytosome Pumpkin-lidocaine was measured by centrifugation by centrifugation technique. The Nano phytosome Pumpkin-lidocaine was separated in the high-speed centrifuge at 4000 rpm for 30 minutes. The sediment was separated from the supernatant. Sediment dissolved in methanol 10 ml, then centrifugation at 4000 rpm for 30 minutes. The entrapment percentage was calculated by the following equation (Hulla et al., 2015).

Entrapment efficiency % = (Entrapped drug /Total drug) ×100

Nano Phytosome Pumpkin-Lidocaine Loaded In The Gel

The gel was made by dissolving 0.125 g of Carbopol in 3 ml of pure distilled water for prepared the gel phase. The acidic component of the gel was then buffered by 1 ml of NaOH 0.1N, which was thoroughly manually blended until being appeared thick and clear. Lastly, the gel was heated for 15 minutes to remove air bubbles (Al-Shati and Ibrahim, 2019). The prepared phytosome was mixed with gel, and 100 mg of Nano phytosome Pumpkin-Lidocaine was mixed with gel 100 mg, to achieve a concentration of 100%.

Nano Phytosome Pumpkin–Lidocaine Standardization

Light Microscope

The light microscope use the visible light to explore the specimen details such as; size and shape, but its ability to resolve very small structures is limited by the wavelength of visible light (Bibi et al., 2011).

The phytosome smear was made; 50 μl of phytosome suspension was examined under the light microscope with an optical filter at an oil immersion magnification scale to characterize the phytosome shape and size. The examination was performed on both Nano phytosome pumpkin and Nano phytosome-pumpkin-lidocaine.

Electron Microscope (Scan And Transmission)

The fundamental principle underlying the electron microscope is akin to that of a light microscope. However, in contrast to utilizing visible light, it employs high-energy electrons as its illumination source (Peddie et al., 2022). Since the specimen interacts with the electron beam, yielding valuable information regarding the phytosome’s size, shape, crystalline structure, transmission for lamellar, and composition (Placzek and Kosela, 2016).

The Nano phytosome pumpkin-lidocaine samples were stored at deep freezing -18°C following packing in sealed Eppendorf tubes. Scanning and transmitted micrographs conducted by (AL-KAK) applied research laboratory submitted to Kashan University in Iran.

X-Ray Diffraction (Xrd)

XRD was used to analyze the crystallographic structure of Nano phytosome pumpkin-lidocaine and ordinary pumpkin seed oil and ordinary lidocaine using an X-ray diffractometer (2 to 40°C) (Udapurkar et al., 2018).

Zeta Potential

zeta potential was used to assess the stability of a dispersion of Nano phytosome pumpkin-lidocaine Nanoparticles (Babazadeh et al., 2018).

Induction Burn Wounds

First, according to the ethical fact, the rabbits were euthanized by infiltration general anesthesia. Clipped electrical shaver machine and shaved the rabbit’s dorsal region with a shaver machine and the prepared area was disinfected with alcohol 70% of the skin was labeled 0.8 cm, at Para-Medline labeled skin area and removed skin layers, burned by pressing the copper tip of an electric soldering tool heated rated to 95 °C and applied for 1 minute to burn wound skin and below to create identical burn wounds, This technique was done to prevent reaching the muscle layer under the skin layers (Giles et al., 2008).

Timeline Analysis Of Burn Wounds Healing

The morphological analysis of new tissue formation was performed at a specific time-point of healing. The closure indices were estimated using three altered parameters as follows:

• Closure rate: the wound closure area per unit time throughout the total growth phase (Jabbar and Al-Bayati, 2022).

• t½ of wound healing: the half-life of closure wound area time in the treated group

t= half-life, q= the intercept, Dc= rate of continuous linear healing, ΔA= alteration in the perceived burn wound area between two measurements, Δt: The time between two specific measurements consecutively

RESULTS AND DISCUSSION

Results

Entrapment %, And Loaded Efficiency % Of Prepared Phytosome

Table (1) showed the entrapment % of Nano phytosome pumpkin-lidocaine and Nano phytosome pumpkin were 95.2 ± 9.41, and 87.32 ± 8.1 respectively, while loaded efficiency% were 86.84 ± 7.77, and 79.40± 3.72 respectively.

 

Table 1: Entrapment%, loaded efficiency%, and Nano size of phytosome.

Phytosome types	Entrapment %	loaded efficiency %	Nano size nm
Nano physiome pumpkin-lidocaine	95.2 ± 9.41a	86.84 ± 7.77 a	79.31 ± 7.20
Nano phytosome pumpkin	87.32 ± 8.1 b	79.40± 3.72 b	71.48 ± 2.24 b

 

The data presented mean ± SE n=5, The different letters denoted (p≤0.05) between types of phytosome.

 

Standardization And Characterization Of Nano Phytosome.

Light microscope and electron micrograph: Fig (1) A and B of the light microscope displayed the primary formation of Nano vesicular shapes of phytosome in each loaded pumpkin seed oil Fig (1) A and pumpkin seed oil with lidocaine formula Fig (1) B. The Nano phytosome pumpkin-lidocaine was examined by scanning electron microscopy (SEM) to determine the phytosome size and spherical shapes distributed homogeneously over a granulation surface representing the Nano phytosome pumpkin particles loaded with lidocaine in the core of the phytosome Fig (2) C, D and E. While Fig (2) A and B showed the transmission electron microscope (TEM) presented the regular distribution of the multilamellar phytosome. Table (1) showed the size of the Nano pumpkin phytosome loading lidocaine and Nano phytosome pumpkin.

 

 

X-Ray Diffraction (X-Rd)

The crystal structure and particle size of prepared crystalline Nanomaterials are determined using the nondestructive method known as XRD. The XRD analysis of ordinary Pumpkin seed oil (PSO) and ordinary lidocaine showed diffraction peaks of different intensities and high in the spectrum, and this is due to the higher crystallinity nature of lidocaine and some of PSO’s active compounds. The main diffraction peaks of ordinary pumpkin seed oil are 2θ =17.63o, 19.94o, 21.59o, 31.45o, 35.92o, 47.11o, 56.15o, 64.55o, and 67.60o while the main peaks of lidocaine are 2θ =23.129, 40.938, 44.432, and 73.958 Fig(3). It was observed that most of the distinctive main diffraction peaks of pumpkin seed oil and lidocaine disappeared from the diffractogram pattern of Nano phytosome pumpkin-lidocaine as compared with ordinary pumpkin seed oil (PSO) and lidocaine, moreover, PSO showed a decrease in the width of the peak diffraction at the range (2θ =17.63o-21.59o) Fig(3).

 

Zeta Potential

The zeta potential was used to clarify and identify the aggregation of Nano phytosome pumpkin-lidocaine due to their small sizes and wide surface area. Fig(4) showed the zeta potential of ordinary pumpkin seed oil, ordinary lidocaine, and Nano phytosome pumpkin-lidocaine were -52.3, -56.4, and -68.3 mV respectively.

Closure Rate And Closure T ½ Of Burn Wound Healing

In general, the wounds treated with Nano phytosome displayed a significantly (p≤0.05) faster closure rate per unit time than negative and positive control groups. The Nano phytosome pumpkin-lidocaine gel 100% and The Nano phytosome pumpkin gel showed significant (p≤0.05) fast values of closure rates 0.216±0.05 and 0.215±0.03 mm/day, respectively as shown in Table (2) and Fig (5&6). On the other hand, negative & positive control groups, and ordinary pumpkin seed oil treated revealed delayed closure rates of 0.021±0.002, 0.023±0.002, and 0.028±0.009 mm/day, respectively Table (2). while the closure t½ of the Nano phytosome pumpkin-lidocaine gel and Nano phytosome pumpkin gel treated groups showed a significant (p≤0.05) decrease in time values. as compared with both -ve &+ve control groups, and ordinary pumpkin seed oil treated group 20.4±1.7, 20.03±2.1, and 18.5±1.1 days, respectively Fig(5 & 6) and Table (2).

 

 

-ve control= negative control

+ve control= positive control

OPSE= ordinary pumpkin seed extract(oil)

Nano PPLG= Nano phytosome pumpkin-lidocaine gel

Nano PPG= Nano phytosome pumpkin gel

 

Table 2: Displays the closure rate in millimeters per day and the time required for half-closure (designated as “Closure t (½) day”) for both the control group and the group receiving treatment throughout 40 days focused on burn wound healing.

Groups	Closure rate mm/day	Closure t (½) day
Negative Control	0.021±0.002e	20.4±1.7 d
Positive Control	0.023±0.002d	20.03±2.1 d
Ordinary pumpkin seed oil	0.028±0.009c	18.5±1.1 c
Nano phytosome pumpkin-lidocaine G 100%	0.216±0.05 a	8.3±1.1 b
Nano phytosome pumpkin G 100%	0.215 ±0.03b	9.1±1.13 a

 

DISCUSSION

Entrapment %, And Loaded Efficiency% Of Prepared Phytosome

The entrapment efficiency serves as a metric to quantify the proportion of pumpkin seed oil (PSO) and lidocaine effectively encapsulated within the Nano phytosome structure. Optimal encapsulation was achieved by forming phytosomes at a 1:2 ratio of phosphatidylcholine (0.5) to pumpkin seed oil (1). This ratio facilitated the creation of electric hydrogen bonds within the polar region of phosphatidylcholine molecules, resulting in an enhanced entrapment efficiency of the pumpkin phytosome, measured at 87.3% ± 8.1. Simultaneously, it allowed for the successful encapsulation of lidocaine within the inner hydrophobic core, achieving an entrapment efficiency of 95.2% ± 9, consistent with the findings of Azeez et al. (2018).

It is important to note that several factors influence the effectiveness of drug encapsulation in phytosomes. These factors encompass characteristics related to both the phytosomes themselves and the drugs intended for encapsulation. Key phytosome-related factors include the preparation process, hydration duration, vesicle lamellarity, solvent properties (including solubility level and pH), membrane rigidity, phospholipid concentration, buffer composition, vesicle size, surface charge, and the nature of the drugs to be encapsulated, be they hydrophilic or lipophilic. These parameters collectively impact the entrapment efficiency of phytosomes, as highlighted by the studies of Lertsutthiwong et al. (2008) and Allawi and Al-Bayati (2020).

Light Microscope And Electron Micrograph

Pumpkin seed oil contains polyphenols, which feature two phenolic hydroxyl groups. These hydroxyl groups bind with the polar choline head of PC, while the lipophilic and nonpolar phosphatidyl group envelops the choline-hydroxyl complex. This unique arrangement results in various charges due to the positive charge of the choline ammonium group in pumpkin seed polyphenols and the negative charge of the phosphate group. This phenomenon leads to the formation of small spherical particles resembling cells (Ghanbarzadeh et al., 2016; Chen et al., 2022).

Several factors have the potential to influence the morphology and configuration of phytosomes. These factors include preparation conditions and time for formation (timely formation being crucial), temperature optimization for enhanced phospholipid binding, the specific medium used for hydration-dehydration, and the exclusive involvement of methanol and chloroform as primary solvents for the formation of large multilamellar Nano formulations. Additionally, the lamellarity of Nano phytosome pumpkin-lidocaine with multilamellar vesicle shape was observed. To achieve multilamellar and stable Nano phytosome formulations, phosphatidylcholine to pumpkin seed oil ratio of 1:2 was selected due to the establishment of electric hydrogen bonds between phosphatidylcholine and pumpkin seed oil, following findings by Saha et al. (2013). Furthermore, temperature and hydration conditions were presumed to impact phytosome lamellarity, as suggested by Gaikwad et al. (2021).

X-Ray Diffraction (X-Rd)

The X-ray diffraction (XRD) profile provides valuable insights into the structural characteristics of Nano phytosome pumpkin-lidocaine. Notably, it reveals the amorphous nature of both pumpkin seed oil (PSO) and lidocaine when encapsulated within the Nano phytosome structure. This is evident in the broadening of the peak signals observed in the XRD pattern. The loss of well-defined peaks for PSO, along with the reduction in their peak width, suggests the formation of a network involving interconnected carbon atoms between the active compounds and phosphatidylcholine within the Nano phytosome (Ghanbarzadeh et al., 2016).

Interestingly, the XRD analysis of Nano phytosome pumpkin-lidocaine exhibited a noteworthy feature—the presence of a significant peak associated with the extract. However, this peak had a lower diffraction intensity compared to ordinary PSO. This observation implies that the interaction between phosphatidylcholine and certain active compounds from the extract may have influenced the degree of crystallinity and intensity within the Nano phytosome, as previously suggested (Pourhojat et al., 2017). This suggests that the PSO loaded in the phytosome structure may have undergone partial recrystallization, resulting in less orderly crystal formation.

Furthermore, the X-ray diffraction spectrum of the loaded lidocaine within Nano phytosome pumpkin-lidocaine displayed considerably weaker diffraction signals compared to ordinary lidocaine. This observation suggests that lidocaine, when encapsulated in the phytosome, assumed a less crystalline structure, aligning with previous findings (Jabbar and Al-Bayati, 2022). This implies that lidocaine within the Nano phytosome is more evenly and consistently distributed within the lipid core at a molecular level, contributing to its reduced crystallinity

Zeta Potential

The zeta potential of nanoparticles is a critical parameter influenced by the chemical nature of stabilizing agents and the pH of the surrounding medium (Lertsutthiwong et al., 2008). In the case of Nano phytosome pumpkin-lidocaine, the measured zeta potential value was -68.3 mV. This value suggests that the combination of pumpkin seed oil (PSO) and lidocaine contributes to a high zeta potential, likely due to an increased number of carboxyl groups. These carboxyl groups have a direct impact on both the size and the negative charge of the nanoparticles (Hatanaka et al., 2010).

The shift towards a negative zeta potential value can be attributed to the incorporation of PSO into the phosphatidylcholine structure. This shift results in a significant increase in the electrostatic repulsion forces between negatively charged particles, effectively preventing particle aggregation. Consequently, this contributes to the exceptional stability of the phytosome and enhances its ability to penetrate the skin (Mora-Huertas et al., 2010;).

Documents noted that other studies have suggested that liposomes loaded with lidocaine, possessing a zeta potential of less than 20 mV, can enhance system stability, reduce the tendency of lidocaine nanoparticles to aggregate, and result in a more controlled release of lidocaine. These findings align with the results obtained in our zeta potential analysis (Jabbar and Al-Bayati, 2022).

Closure Rate, And Closure T ½ Of Burn Wound

Numerous studies have documented the positive impact of pumpkin seed oil (PSO) on wound healing, particularly in accelerating the initial stages of the process (Rezk et al., 2023). The mechanisms through which PSO facilitates wound healing when applied topically are multifaceted. These mechanisms likely involve its potent antioxidant activity, anti-inflammatory properties, promotion of re-epithelialization, stimulation of fibroblast differentiation and migration, up-regulation of growth factors such as TGF-beta, neovascularization, promotion of collagen synthesis, wound shrinkage, and tissue remodeling (Fahmi et al., 2014;).

One noteworthy component of PSO is its high content of linoleic acid, which serves as the precursor to arachidonic acid (Siano et al., 2016). Arachidonic acid is a primary polyunsaturated fatty acid found in the skin and plays a pivotal role in modulating and expediting the inflammatory process, it achieves this by generating key inflammatory mediators like leukotrienes, thromboxane, and prostaglandins. These mediators, in turn, enhance wound healing by facilitating local neovascularization, fibroblast differentiation, cellular migration, and extracellular matrix remodeling (Bardaa et al., 2016b).

Moreover, the antioxidant properties of PSO likely contribute to wound healing by safeguarding cells against damage, increasing vascularity, and strengthening collagen fibers (Kaur et al., 2019). PSO may further enhance wound healing by stimulating and increasing fibroblast formation, migration, and mitogenesis during the proliferation phase. Consequently, as fibroblasts increase, there is a corresponding rise in collagen deposition within the dermis, particularly collagen types I and II (Al Chalabi et al., 2021).

PSO may expedite wound closure by promoting re-epithelization through the elevation of growth factors such as Keratinocyte Growth Factor (KGF) and interleukin-6 (Bardaa et al., 2016). When PSO is formulated into nanoparticles, it appears to intensify its therapeutic effects, achieving comparable results to those obtained with conventional PSO. This enhancement could be attributed to the small size of nanoparticles, which facilitates deeper penetration into the skin with increased permeability, targeting the active site and enabling a higher concentration (Susilawati et al., 2021).

Additionally, the incorporation of lidocaine into the core of the phytosome structure provides a sedative effect and offers short-term relief from itching during the treatment period. This, in turn, contributes to improved wound healing and reduces the frequency of dressing changes (Jabbar and Al-Bayati, 2022).

CONCLUSIONS AND RECOMMENDATIONS

Reformulated the pumpkin seed oil to Nano phytosome pumpkin-lidocaine demonstrated good physical stability, Reducing the crystal nature of active extract substances and improving the entrapment efficiency %. The Nano phytosome pumpkin-lidocaine gel 100% and Nano phytosome pumpkin gel 100% showed significant acceleration and diminished closure rate and closure t ½ of the burned wound as compared with ordinary pumpkin oil treated group and both positive, and negative control groups.

Application of the formula to humans and large animals for burned wounds, as well as can be used for recovery during the remodeling phase in different degrees of external wound

ACKNOWLEDGEMENTS

We do thank and praise Allah as thankers and praisers thanking and praising for the guidance and aid in finishing this paper. He is the first and last deserver of thinking and praising. A special thanks and gratitude to the pharmacology and toxicology department, college of veterinary medicine/the University of Baghdad, State Company for Drug and medical appliance/Samarra Department of Pharmacology, for consultation and for facilitating particular challenges of the work.

CONFLICT OF INTEREST

The authors have declared no conflict of interest.

DATA AVAILABILITY

Authors will provide all data at the reasonable request.

NOVELTY STATEMENT

The preliminary study formulated Nano-phytosomes with Pumpkin Seed Oil in a burn wound in the full third stage on the skin with analgesic lidocaine for accelerating healing with low adverse effects during the healing phase and remodeling phase.

AUTHORS’ CONTRIBUTION

First author: practical work and search writing

Second author: Implant and suggested project and methodology writing

Third author: final arrangement and styling.

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