Name: Ocular Therapeutic Delivery and Advanced Tissue Retrieval in Adult Rats (Video) | JoVE Journal
Uploaded: 2025-05-23T13:45:00.000+00:00
Duration: 6 min 30 s
Description: Learn retrobulbar injection techniques for ocular drug delivery and en bloc tissue retrieval in adult rats. This standardized protocol enables therapeutic intervention and analysis of posterior ocular tissues.

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5 minutes

This work was partially funded by US Department of Defense Vision Research Program Awards W81XWH-15-1-0074 and W81XWH-22-1-0989. The opinions or assertions contained herein are the private views of the authors and are not to be construed as official or as reflecting the views of the Department of the Army or the Department of Defense. This research grant was supported in part by the Ohio Affiliate of Prevent Blindness Young Investigator Student Fellowship Award for Females Scholars in Vision Research. We gratefully acknowledge support from the Ross Foundation. Services were performed at the OSU Vision Sciences Research Core Program under P30EY032857. We would like to thank The Ohio State University Laboratory and Animal Resources (ULAR). In addition, we would like to thank Reilly undergraduate lab members Michelle Mosko, Emma Lally, Sam Duckworth, and Eve Howard. We would also like to thank Bongsu Kim for contributing to the SALOOT design, as well as Elizabeth Urbanski and Ryan Webb. Figure 1, Figure 2A, and Figure 3 were created with BioRender.com.

All experiments were conducted in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Visual Research and approved by the institutional animal care and use committee at Ohio State University. Male Sprague Dawley rats weighing ~200 g and around 2 months of age were used for this study25. Details of the reagents and the equipment used are listed in the Table of Materials.
1. Intravitreal injection (IVI)
<ol>
	<li>Attach the isoflurane and waste leads to the SALOOT attachment ports. Anesthetize the animal using standard isoflurane procedures following the ARVO Statement for the Use of Animals in Ophthalmic and Visual Research and approved IACUC protocol. 
	NOTE: Alternatively, if the animal was already under anesthesia from another ophthalmic testing session (i.e., ketamine/xylazine mix; 90 mg/kg ketamine and 10 mg/kg xylazine), transfer the animal to the ophthalmic surgery platform and titrate anesthesia with isoflurane (1-4%) delivered with oxygen (0.5-1 L/min flow rate) to ensure adequate depth of anesthesia is maintained.</li>
	<li>Place the ophthalmic surgery platform with the anesthetized animal under a live operating microscope. Assess the anesthetic depth via pedal withdrawal reflex.</li>
	<li>Place two drops of 0.5% tetracaine hydrochloride ophthalmic solution (topical anesthetic) into the eye or eyes being operated on. Apply lubricating topical ophthalmic ointments such as hypromellose 0.3% to the contralateral eye if no manipulation is to be performed. 
	NOTE: Lubricating topical ophthalmic ointment is not added to the eye being manipulated prior to the procedure to ensure clear visualization during the procedure and distribution of the tetracaine solution. Lubricating ointment may be applied following the procedure.
	<ol>
		<li>Then, use one to two drops of 5% povidone-iodine on the ocular surface, and using a cotton swab, apply povidone-iodine to the skin surrounding the eye.</li>
	</ol>
	</li>
	<li>Use a 10 &#181;L syringe with a 33 G needle with a style 4 tip at a length of 10 mm and angle of 15 degrees and draw up 0.9% bacteriostatic sodium chloride. Flush the syringe and needle with the saline before dipping the needle into a hot bead sterilizer.
	<ol>
		<li>Allow it to cool before proceeding. After the needle has cooled, draw up the therapeutic of interest to the desired amount (4 &#181;L). 
		NOTE: For proof of concept studies, non-dilute tattoo ink and Evan&#39;s Blue dye in phosphate-buffered saline (PBS) were utilized. Evan&#39;s Blue powder was mixed with PBS until opaque. For therapeutic proof of concept studies, the following concentrations were utilized: ibudilast at 1 mg/mL, tauroursodeoxycholic acid (TUDCA) 5 mg/mL, cyclosporine injection, 250 mg/mL, and anakinra 100 mg/0.67 mL. Therapeutic powders were diluted in 0.9% bacteriostatic saline.</li>
	</ol>
	</li>
	<li>Using fine ophthalmic forceps with teeth, gently grasp the scleral tissue at the limbus to stabilize. There will be a faint red ring around the iris. Use this ring as a landmark, insert the needle, bevel side down, and inject it into the posterior eye. 
	NOTE: Ensure to angle the needle towards the retina and only insert the needle 2/3 of the way (Figure 1). Ensure the needle does not scratch the lens, as this will lead to cataract formation.</li>
	<li>After the therapeutic has been injected, slowly remove the needle. Close the eye and hold pressure for at least 10-15 s before flushing with saline.</li>
	<li>Discontinue the animal from isoflurane and remove it from the ophthalmic surgery platform. Place a drop of hypromellose 0.3% in each eye and then allow the animal to recover on a heating pad.</li>
</ol>
2. Retrobulbar injection (RBI)
<ol>
	<li>Attach the isoflurane and waste leads to the SALOOT attachment ports. Anesthetize the animal using standard isoflurane procedures. 
	NOTE: Alternatively, if the animal was already under anesthesia from another ophthalmic testing session (i.e., ketamine/xylazine mix; 90 mg/kg ketamine and 10 mg/kg xylazine), transfer the animal to the ophthalmic surgery platform and titrate anesthesia with isoflurane (1-4%) delivered with oxygen (0.5-1 L/min flow rate) to ensure adequate depth of anesthesia is maintained.</li>
	<li>Place the ophthalmic surgery platform with the anesthetized animal under a live operating microscope. Assess the anesthetic depth via pedal withdrawal reflex.</li>
	<li>Place two drops of 0.5% tetracaine hydrochloride ophthalmic solution (topical anesthetic) into the eye or eyes being operated on. Apply lubricating topical ophthalmic ointments such as hypromellose 0.3% to the contralateral eye if no manipulation is to be performed. 
	NOTE: Lubricating topical ophthalmic ointment is not added to the eye being manipulated prior to the procedure to ensure clear visualization during the procedure and distribution of the tetracaine solution. Lubricating ointment may be applied following the procedure.
	<ol>
		<li>Then, use one to two drops of 5% povidone-iodine on the ocular surface and using an eye spear, apply povidone-iodine to the skin surrounding the eye.</li>
	</ol>
	</li>
	<li>Obtain a 0.5 mL insulin syringe with a 28 G needle. Draw up the therapeutic of interest to the desired amount (100 &#181;L). 
	NOTE: For proof of concept studies, non-dilute tattoo ink and Evan&#39;s Blue dye in phosphate-buffered saline (PBS) were utilized. Evan&#39;s Blue powder was mixed with PBS until opaque. For therapeutic proof of concept studies, the following concentrations were utilized: ibudilast at 10 mg/mL, TUDCA at 50 mg/mL, cyclosporine injection 250 mg/mL, and anakinra at 100 mg/0.67 mL. Therapeutic powders were diluted in 0.9% bacteriostatic saline.</li>
	<li>Using fine ophthalmic forceps with teeth, gently grasp the lower eyelid to stabilize. Insert the needle, bevel side down, at an angle halfway between 6 and 7 o&#39;clock along the lower orbital rim until the back of the ocular socket is felt. Pull the needle back slightly and then slowly inject the therapeutic (Figure 2).</li>
	<li>Gently and slowly remove the needle. Then, close the eye and hold pressure for at least 10-15 s before flushing with saline.</li>
	<li>Discontinue the animal from isoflurane and remove it from the ophthalmic surgery platform. Place a drop of hypromellose 0.3% in each eye and then allow the animal to recover on a heating pad.</li>
</ol>
3. Ocular tissue isolation dissection
<ol>
	<li>After the animal has been euthanized via CO2 asphyxiation or as otherwise stated in approved IACUC Protocol, place the animal in sternal recumbency. Utilize a transverse skin incision over the dorsal neck, extending to the level of the ear pinna.</li>
	<li>Dissect dorsal musculature to expose the atlanto-occipital joint. Use mayo scissors to incise through the atlanto-occipital joint, separating the head from the body (Figure 3). Using blunt dissection, gently remove the skin from the dorsal cranium from the level of the nose to the dorsal neck, leaving the skin around both eyes intact.</li>
	<li>Insert a pair of medium straight hemostats or needle drivers into the foramen magnum at the base of the skull. Use the hemostats to gently break through the lateral skull extending from the foramen magnum to the temporal region on both sides (Figure 3).
	<ol>
		<li>When removing the top of the skull, keep the hemostats parallel to the dorsal side of the brain. This will ensure the brain remains intact and is not nicked in the bone removal process.</li>
	</ol>
	</li>
	<li>Using a flat spatula, gently reflect the brain rostrally to expose optic nerves. Care must be taken so that tension from the weight of the brain is not applied to the optic nerves.</li>
	<li>With the nerves exposed, take a pair of medium microscissors and make a small incision across the optic chiasm, severing both nerves from the brain. At this point, the brain can be discarded or placed in paraformaldehyde in PBS (4% PFA) for 24 h at 4 &#176;C for histological assessment.</li>
	<li>Using a pair of small iris scissors and a pair of toothed ophthalmic micro forceps, carefully remove the excess tissue (i.e., eyelids, connective tissue, etc.) from around the eye. Once completed, the eye should be situated in the ocular socket but with only the extraocular muscle and glands still present.</li>
	<li>Using the hemostats in conjunction with the small iris scissors, cut through the ocular orbit, taking great care not to cut into the optic nerve as it passes through the optic canal. Carefully break away the bone at the back of the ocular socket with the hemostats, and for more precise control, utilize the small dissection scissors.</li>
	<li>After the bone has been removed, delicately cut around the ocular orbit with a pair of microscissors and fine forceps to remove the fat pads, glands, and extraocular muscles. Ensure to be observant of the optic nerves during this process.</li>
	<li>The eye should be able to be gently reflected caudally towards the interior of the skull. At this point, use small microscissors and fine forceps to remove the connective tissue surrounding the nerve on the lower skull ridge.</li>
	<li>Once this tissue has been removed, the eye and full optic nerve should be able to be lifted from the skull en bloc. Repeat these steps for the contralateral eye and nerve.</li>
	<li>Further, clean the optic nerve and eye of excess tissue such as the dural sheath. If tissues do not need to be preserved for histological analysis, then flash freeze using dry ice or liquid nitrogen before being stored at -80 &#176;C.</li>
	<li>For mass spectrometry, the retina needs to be isolated from the internal region of the globe, and the optic nerve needs to be isolated. Separate the optic nerve from the globe at the closest exterior point. Place the nerve in a cryotube on ice before being transferred to -80 &#176;C.
	<ol>
		<li>Place the globe of the eye on a Petri dish under an operating microscope. Use a pair of curved forceps to hold the eye steady before making an incision at the limbus with a pair of small microscissors.</li>
		<li>Extend the cut to encompass the entire circumference of the globe. The globe should be bisected, and the anterior portion can be discarded.</li>
		<li>Place the posterior section interior side up, and using a pair of fine ophthalmic tweezers, remove the thin cream-colored tissue. It may appear to stick to the optic disc. If this occurs, use the microscissors to cut the retina away from the disc. 
		NOTE: The retinal tissue can then be placed in a cryotube on ice before transferring to -80 &#176;C. Tissues can then be transferred to the mass spectrometry facility for evaluation.</li>
	</ol>
	</li>
	<li>For immunohistology staining using partial perfusion, place the intact eye on a Petri dish. Use a pair of curved forceps to hold the eye steady before taking an insulin syringe with a 28 G needle and inserting it at the limbus, with the needle angled towards the retina. Repeat this step at another two points along the limbus. Puncture of the globe helps to ensure adequate perfusion and aids in appropriate fixation. 
	NOTE: The globe should be fixed in 4% PFA for at least 40 min prior to transitioning to a shaker and agitating at low speed for an additional 20 min to facilitate fluid movement.</li>
	<li>Once the fixation step is complete, remove the PFA and replace it with PBS. Place vials on gentle shake for 15 min, and then repeat this step for a second 15 min PBS rinse.</li>
	<li>After the final PBS rinse cycle, aspirate out the PBS and replace it with 30% sucrose solution in PBS, and then refrigerate for 24 h. Following the sucrose incubation step, embed tissue in OCT for histological evaluation26.</li>
</ol>

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The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

The intricate challenges associated with delivering therapeutics to the retina and optic nerve, primarily due to the impermeable barrier posed by the BRB, underscore the significance of this study3,4. The exploration of IVI and RBI techniques not only highlights innovative approaches for overcoming these obstacles but also emphasizes the broader implications for ocular care and therapeutic development. These findings demonstrate that both IVI and RBI can facilita...

Delivering therapeutics to the retina and optic nerve is incredibly difficult due to the complex anatomy of the eye1,2, specifically the presence of the blood-retinal barrier (BRB)3,4,5. The BRB serves to protect the retina from systemic circulation invasion, but is a challenging opponent to therapeutic administration as systemic therapeutic circulation is often blocked by the BRB6,7. Small lipophilic molecules can readily diffuse through the BRB, but larger and hydrophilic molecules have a harder time gaining access to the retina6. Intravitreal (IVI) and retrobulbar (RBI) injections enable the delivery of drugs to the ocular tissues, overcoming the limitations imposed by the BRB. The IVI serves as a promising compromise by administering therapeutics into the internal environment of the eye8,9. This method requires the drug to cross through the vitreous, thus bypassing the BRB, and diffusing through the retina and choroid in order to reach the optic nerve7. The RBI is delivered behind the eye into the retrobulbar space10. Therapeutics can be delivered by diffusion through the tissues and glands in the retrobulbar space, affecting the optic nerve and surrounding structures without directly entering the retina, which maintains the integrity of the BRB. By delivering drugs directly or indirectly into the eye, both intravitreal and retrobulbar injections can achieve higher local concentrations of the therapeutic drug, which enhances its effectiveness compared to topical or systemic administration (oral or intravenous)2. This is particularly important for treatments that require rapid action or high potency, as seen in many ocular diseases. Targeted delivery also limits the exposure of the rest of the body to the drug, which reduces the risk of off-target effects and helps to minimize potential adverse effects that can occur when medications are administered topically, orally, or intravenously11.
Other periocular injections, such as subconjunctival, posterior subtenon, and subretinal, have their own benefits and limitations2,5. Posterior subtenon injections have been observed to deliver high drug concentrations to ocular tissues; however, the subtenon injection is closer to the scleral than the orbital vasculature5,12. In contrast, the RBI places the therapeutic closer to the optic nerve than the posterior subtenon or subconjunctival13. This may mean that optic nerve pathologies favor RBI-delivered therapeutics over other periocular injection types. Posterior subtenon injections have associated risks, including strabismus, hyphema, and elevated intraocular pressure5. Elevated intraocular pressure is also a reported risk factor in IVI, subconjunctival, and subretinal injections2. These injection types often require repetitive dosing in order to achieve the desired therapeutic effect2. Other risk factors associated with subretinal injections, subconjunctival injections, and IVI include cataract formation, retinal hemorrhage, retinal detachment, and inflammation2. These IVI, subretinal injections, and subconjunctival injections are more invasive than the RBI injections, as these injections are intraocular2. The RBI may be considered less invasive as it places the therapeutic in the retrobulbar space, without directly entering the needle into the globe of the eye. Other less invasive therapeutic delivery strategies, such as topical administration, fall short of sufficient drug delivery, with less than 5% of the drug being retained on the ocular surface2,5.
IVI is a prominent technique in preclinical models that is used for its ability to deliver therapeutic agents directly into the posterior segment of the eye. IVI delivers the drug directly to the vitreous humor, making it a preferred delivery technique for localized treatment14. The IVI technique allows the therapeutic to bypass the blood-retinal barrier, which is a common hindrance to drug penetration into the retina14. IVI introduces the opportunity for inflammation and damage to ocular structures, so meticulous adherence to the procedure must be employed14. To minimize retinal detachment and cataract formation, Chiu et al. describe an IVI approach that emphasizes a 45-degree bevel insertion and injection at the level of the par plana, avoiding the lens, retina, ocular muscle, and vessels15. In this technique, a 30 G needle is inserted into the nasal sclera for therapeutic delivery15. IVI is still associated with risks due to its invasive nature. Potential risks include retinal detachment, cataract formation, endophthalmitis, or hemorrhage16. The invasive nature of IVI techniques also increases intraocular pressure, as shown in an experiment on porcine eyes performed by Ikjong Park et al.16. The study shows changes in intraocular pressure during different stages of needle insertion and fluid injection. They report substantial variation in intraocular pressure during the procedure16.
RBIs have been successfully utilized in previous studies as a means of therapeutic delivery to rodents. One such study compared the effects of various prostaglandin analogs given via RBI17. Albino rats were given an RBI with a 26 G needle of 0.1 mL injectate inserted through the lateral area of the inferior fornix at a 45-degree angle17. The protocol used in this study was adapted from a previously described method in which the rats were anesthetized via intraperitoneal (IP) injection of chloralhydrate18. Another study conducted on rats compared topical drops to retrobulbar injections19. The rats were anesthetized via an IP injection of ketamine/xylazine, and the RBI was given via a 30 G needle19. In contrast to the previously discussed sedation methods, one study observing the effects of RBI on orbital fat used inhalational isoflurane to sedate the rats prior to RBI20. While these studies provide insight into what anesthetics and needle specifications could be successful, the positioning and handling of the animals during the procedure are not discussed.
Various studies in mice also conduct RBIs for therapeutic delivery methods. One study compared RBI to lateral tail vein injection for successfully inducing nephrotic syndrome21. A second study also compared the same two injection techniques in the administration of contrast media for cardiac imaging22. The mice were anesthetized with inhalational isoflurane and injected in the medial side of the eye22. Both studies adapted their RBI method from a previously written protocol. It is important to note that this protocol named their injection as retro-orbital yet described the injection location as the retrobulbar space behind the eye. The authors of this protocol utilized inhalational isoflurane as a preferred sedation method, noting the quick activation and recovery time of the mice23. For an RBI, the eye was partially protruded from the socket by applying pressure to the skin around the eye23. Then, the needle was introduced at the medial canthus bevel side down at an angle of 30 degrees and was inserted until it reached the base of the eye23. Care must be taken when applying pressure to the animal, as accidental blood flow blockage or tracheal collapse may occur23. The injector is also blind to the needle tip upon insertion, and therefore, damaging the eye is an associated risk.23 Damaging the eye upon therapeutic administration is a critical risk in this experiment, as causing additional injury directly undermines the results of the study. It also must be noted that the positioning and handling technique previously described was conducted on mice and did not include comments on applicability to rats.
There are many manners in which optic nerve and retina removal have been attempted. One such method explored the removal of optic nerves and eyes en bloc, preserving an intact optic chiasm24. This method is the most comparable to the current study as the individual eyes and optic nerves are also preserved for en bloc removal; however, the optic chiasm is separated. Exercising caution in this procedure would be of the utmost importance due to the complexity of the procedure. In the current method, we begin the dissection via the caudal skull and work rostrally in order to provide access in a way that limits damage to the optic nerves and allows the entire nerve to remain intact. Furthermore, keeping the nerve intact and attached to the eye is crucial to the embedding process, as damage to each part of the nerve can correspond to a different pathological observation24. The orientation of the optic nerve is important to consider as how it is embedded allows for different cross sections, which may be important for histological analysis.
A custom-made device known as the small animal laboratory ophthalmic operating table (SALOOT, an ophthalmic surgery platform) is comprised of a series of 3D printed materials to provide anesthesia and hold the animal in a stable position for ocular therapeutic injections. The SALOOT design allows for stability of the head and ocular structures for ophthalmic procedures, which improves the speed and reproducibility of operations while allowing for gas anesthesia delivery and scavenging of exhalation particulates. The SALOOT is a three-dimensional printed block featuring a concave reduction to hold the rat body with a narrower region at the front to hold the head of the animal into a nose cone with an isoflurane inlet. Beneath the nose cone is a small reservoir and exhaust outlet. The following methods were developed for therapeutic ocular delivery and precise ocular tissue retrieval; they were designed for studying tissues after ocular trauma, so it is crucial to delineate the effects of the trauma, injection, treatment, and dissection to avoid confounded interpretation of findings.
This article presents two ocular therapeutic injection methods, the intravitreal and retrobulbar injections, for use in adult rats. In addition, a tissue retrieval method is presented for the en bloc removal of the intact optic nerve and retina from an adult rat. These techniques enable the investigation of ocular and peri-ocular effects of induced pathology and treatment.

<table><tbody><tr><td>Anakinra 100 mg/0.67 mL&amp;nbsp;</td><td>Sobi</td><td>NDC: 66658-0234-07</td><td></td></tr><tr><td>Antipamezole hydrochloride (Antisedan) 5.0 mg/mL</td><td>Zoetis</td><td>NADA #141-033 | 107204-8</td><td></td></tr><tr><td>Bacteriostatic sodium chloride (0.9%)</td><td>Hospira Inc.</td><td>NDC: 0409-1966-02</td><td></td></tr><tr><td>Cryotube</td><td>VWR</td><td>76417-258</td><td>&amp;nbsp;https://us.vwr.com/store/product?keyword=76417-258</td></tr><tr><td>Curved forceps&amp;nbsp;</td><td>Fischer Scientific&amp;nbsp;</td><td>08-953F</td><td></td></tr><tr><td>cyclosporine injection 250 mg/mL&amp;nbsp;</td><td>Perrigo</td><td>NDC: 00574-0866-10</td><td></td></tr><tr><td>cyclosporine topical, 0.05% (Restasis)&amp;nbsp;</td><td>AbbVie (Vizient)</td><td>NDC: 00023-9163-30</td><td></td></tr><tr><td>Cyotube Cap</td><td>Thermo Scientific</td><td>3471BLK</td><td>https://www.fishersci.com/shop/products/screw-cap-microcentrifuge-tube-caps/14755237?searchHijack=true&amp;amp;searchTerm=&lt;br/&gt; screw-cap-microcentrifuge-tube-caps&amp;amp;searchType=Rapid&amp;amp;&lt;br/&gt; matchedCatNo=14755237</td></tr><tr><td>Evans Blue&amp;nbsp;</td><td>Sigma-Aldrich</td><td>E2129-10G</td><td></td></tr><tr><td>Eye Spears</td><td>Fischer Scientific&amp;nbsp;</td><td>NC0972725</td><td>https://www.fishersci.com/shop/products/ultracell-pva-eye-spears-100-p/NC0972725</td></tr><tr><td>Fine forceps&amp;nbsp;</td><td>Fischer Scientific&amp;nbsp;</td><td>08-953E</td><td>https://www.fishersci.com/shop/products/fisherbrand-dissecting-jewelers-microforceps-2/08953E?gclid=Cj0KCQiAkJO8BhCGARIsAM&lt;br/&gt; kswyiER9Kanmi3ZMgoXTr82Zg3&lt;br/&gt; g44m1Q6WLftkYfb36hC7pbkwR&lt;br/&gt; hVAy3MaAqkLEALw_wcB&amp;amp;ef_id&lt;br/&gt; =Cj0KCQiAkJO8BhCGARIsAMks&lt;br/&gt; wyiER9Kanmi3ZMgoXTr82Zg3g4&lt;br/&gt; 4m1Q6WLftkYfb36hC7pbkwRhV&lt;br/&gt; Ay3MaAqkLEALw_wcB:G:s&amp;amp;ppc&lt;br/&gt; _id=PLA_goog_2086145680_81&lt;br/&gt; 843405274_08953E__38624700&lt;br/&gt; 1354_6556597232892883360&amp;amp;&lt;br/&gt; ev_chn=shop&amp;amp;s_kwcid=AL!4428&lt;br/&gt; !3!386247001354!!!g!827721591&lt;br/&gt; 040!&amp;amp;gad_source=1</td></tr><tr><td>Fine ophthalmic forceps with teeth&amp;nbsp;</td><td>Fisher Scientific</td><td>50-253-8287</td><td>https://www.fishersci.com/shop/products/bonn-suturing-forceps-7-5-cm/502538287</td></tr><tr><td>Flat spatula&amp;nbsp;</td><td>Fischer Scientific&amp;nbsp;</td><td>14-375-100</td><td>https://www.fishersci.com/shop/products/fisherbrand-spoonula-lab-spoon/1437510#?keyword=</td></tr><tr><td>Hot bead Sterilizer&amp;nbsp;</td><td>Fine Science Tools</td><td>18000-45</td><td>https://www.finescience.com/en-US/Products/Instrument-Care-Accessories/Sterilization/Hot-Bead-Sterilizers</td></tr><tr><td>Hypromellose 0.3% (GenTeal Tears Severe Dry Eye Gel)&amp;nbsp;</td><td>Alcon Laboratories Inc.</td><td></td><td>https://www.amazon.com/GenTeal-Tears-Lubricant-Ointment-Night-Time/dp/B01IN5G1L0/ref=sr_1_4?dib=eyJ2IjoiMSJ9.DxYpqjIIBNO&lt;br/&gt; TVuPo7jln5xeGazA_YFg0cbt3&lt;br/&gt; kCyC-0ouZARw5qIHYvCM7vB&lt;br/&gt; R_vO30OWUEXDZhQmQfLQ9&lt;br/&gt; 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cpc&amp;amp;utm_campaign=8674694095&lt;br/&gt; &amp;amp;utm_content=105162454052&amp;amp;&lt;br/&gt; gad_source=1&amp;amp;gclid=Cj0KCQiA&lt;br/&gt; kJO8BhCGARIsAMkswygXXfgY&lt;br/&gt; ABr7EfLtf4tvuLS0E8A4SxX4XM&lt;br/&gt; NJQDaI80Yi4FO-iahCsPcaAp9E&lt;br/&gt; EALw_wcB</td></tr><tr><td>phosphate-buffered saline (PBS)</td><td>Sigma-Aldrich</td><td>P3813-10PAK</td><td>https://www.sigmaaldrich.com/US/en/product/sigma/p3813</td></tr><tr><td>Povidone-Iodine (Betadine) 5%&amp;nbsp;</td><td>Alcon Laboratories Inc.</td><td>NDC: 0065-0411-30</td><td></td></tr><tr><td>Shaker Model 3500&amp;nbsp;</td><td>VWR</td><td>89032-092</td><td></td></tr><tr><td>Small iris scissors&amp;nbsp;</td><td>Sigma-Aldrich</td><td>Z265977-1EA</td><td>https://www.sigmaaldrich.com/US/en/product/aldrich/z265977&amp;amp;</td></tr><tr><td>small microscissors&amp;nbsp;</td><td>Fisher Scientific</td><td>17-456-004</td><td>https://www.fishersci.com/shop/products/self-opening-scissors-2/17456004?keyword=true</td></tr><tr><td>Sprague Dawley Rat</td><td>Charles River Laboratories International, Inc.</td><td>SAS 400</td><td>https://emodels.criver.com/product/400</td></tr><tr><td>Sucrose&amp;nbsp;</td><td>Millipore Sigma</td><td>57-50-1</td><td>https://www.sigmaaldrich.com/US/en/substance/sucrose3423057501</td></tr><tr><td>syringe 10 &amp;micro;L (Model 701 RN)</td><td>Hamilton</td><td>80330</td><td></td></tr><tr><td>Tattoo Ink (Intenze Tattoo Ink True Black 1 oz)</td><td>Amazon</td><td></td><td>https://www.amazon.com/Intenze-Tattoo-Ink-True-Black/dp/B01GW747L2</td></tr><tr><td>tauroursodeoxycholic acid (TUDCA)&amp;nbsp;</td><td>Milipore Sigma</td><td>580549-1GM</td><td></td></tr><tr><td>Tetracaine Hydrochloride Ophthalmic Solution 0.5%</td><td>Bausch &amp;amp; Lomb Inc.</td><td>NDC: 68682-920-64</td><td></td></tr><tr><td>Xylazine (Rompun) 100 mg/mL</td><td>Dechra</td><td>NADA #047-956 |</td><td></td></tr></tbody></table>

ocular therapeutic delivery and advanced tissue retrieval in adult rats

Ocular Therapeutic Delivery and Advanced Tissue Retrieval in Adult Rats

Therapeutic delivery to the posterior segment of the eye, including the retina and optic nerve, is complicated by the presence of blood-brain and blood-retinal barriers. Small animal models, such as rats, are utilized for studying various ocular pathologies. While therapeutic delivery to the posterior eye is challenging, achieving it is essential for treating ocular disorders, many of which require validation in small animal models for translational relevance. Therefore, two posterior therapeutic delivery techniques are presented: intravitreal injection (IVI) and retrobulbar injection (RBI) for use in adult rats. Additionally, a method for the en bloc removal of the eyes and optic nerves is introduced for various histological and molecular analysis techniques. The dissection protocol enables full observation of the neuro-visual system while minimizing post-mortem injury to retinal and optic nerve tissues. Successful delivery of the therapeutic cyclosporine to the retina and optic nerve was achieved, with detectable concentrations observed twenty-four hours after injection using both IVI and RBI. Furthermore, en bloc retina and nerve samples were successfully extracted for full eye histological tissue analysis, facilitating comprehensive observation of the retina and the wider neuro-visual system.

Preliminary pilot experiments were performed on cadaver animals using injection dye (Evans Blue dye) and tattoo ink (Figure 2B) to optimize the placement and size of the needle for both RBI and IVI. Tattoo ink was non-dilute, and then Evans Blue powder was mixed in PBS until the fluid became opaque. We concluded the ideal RBI featured a 28 G needle inserted at an angle halfway between 6 and 7 o'clock along the lower orbital rim until the back of the ocular socket was felt. This delivered the...

This study presents a methodology for the delivery of therapeutics into the retina and optic nerves of the adult rat. Additionally, a unique tissue retrieval method is introduced for a top-down en bloc collection of the optic nerve and retina in an adult rat.

Therapeutic delivery to the posterior segment of the eye, including the retina and optic nerve, is complicated by the presence of blood-brain and ...

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Research

JoVE Journal

Neuroscience

This paper details how Elvax 40W can be used as a slow-release method for drug delivery to the adult rat retina. The protocol for preparing, loading, and delivering the drug-resin complex to the eye is described.

Slow-release Drug Delivery through Elvax 40W to the Rat Retina: Implications for the Treatment of Chronic Conditions

Direct injection into the rat optic nerve is useful for regenerative research. We demonstrate a minimally-invasive technique for direct injection into a rat optic nerve that does not involve opening the skull. Using this method, surgical complications are minimized and recovery is more rapid.

Minimally-invasive Technique for Injection into Rat Optic Nerve

The goal of this protocol is to photochemically induce ischemic injury to the posterior optic nerve in rat. This model is critical to studies of the pathophysiology of posterior ischemic optic neuropathy, and therapeutic approaches for this and other optic neuropathies, as well as of other CNS ischemic diseases.

Rat Model of Photochemically-Induced Posterior Ischemic Optic Neuropathy

Subretinal injection has been widely applied in preclinical studies of stem cell replacement therapy for age-related macular degeneration. In this visualized article, we describe a less risky, reproducible and precisely modified subretinal injection technique via the trans-scleral approach to deliver cells into rat eyes.

Development of a Refined Protocol for Trans-scleral Subretinal Transplantation of Human Retinal Pigment Epithelial Cells into Rat Eyes

Secondary degeneration of retinal ganglion cells (RGCs) occurs commonly in glaucoma. This study describes an innovative operative approach for partial optic nerve transection. The use of this space-saving operative approach extends the model's application range, and allows exploration of secondary injury mechanisms in RGCs in a new way.

Partial Optic Nerve Transection in Rats: A Model Established with a New Operative Approach to Assess Secondary Degeneration of Retinal Ganglion Cells

The goal of this protocol is to characterize a novel model of glaucomatous neurodegeneration based on 360° thermic cauterization of limbal vascular plexus, inducing subacute ocular hypertension.

Full-Circle Cauterization of Limbal Vascular Plexus for Surgically Induced Glaucoma in Rodents

This protocol describes a technique for intracameral injection in rats using a central corneal incision and a long tunnel into the anterior chamber. This injection method minimizes the risk of inducing inadvertent tissue damage and thereby improves precision and reproducibility.

Intracameral Injection in Rats with Low Risk of Adverse Effects

This article describes methods for subretinal injection in rats, utilizing intraoperative visualization to control both the injection site and the area of retinal detachment.

Intraoperative Visualization of Subretinal Injection and Retinal Detachment in Rats

This protocol describes a unique technique using a transconjunctival approach to access the rat optic nerve for injections.

Transconjunctival Approach for Injection into the Rat Optic Nerve

We describe a technique for the preparation of clarified human cortical homogenates, protein separation by SDS-PAGE, antigen retrieval and immunoblotting with an antibody to the Aβ peptide. Using this protocol, we consistently detect monomeric and multimeric Aβ in cortical tissue from humans with Alzheimer's pathology.

SDS-PAGE/Immunoblot Detection of A&beta; Multimers in Human Cortical Tissue Homogenates using Antigen-Epitope Retrieval

Learn retrobulbar injection techniques for ocular drug delivery and en bloc tissue retrieval in adult rats. This standardized protocol enables therapeutic intervention and analysis of posterior ocular tissues.

Ocular Therapeutic Delivery and Advanced Tissue Retrieval in Adult Rats

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