Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

A novel flexible microfluidic meshwork to reduce fibrosis in glaucoma surgery

  • Behzad Amoozgar ,

    Contributed equally to this work with: Behzad Amoozgar, Xiaoling Wei

    Affiliation Department of Ophthalmology, University of California, San Francisco, California, United States of America

  • Xiaoling Wei ,

    Contributed equally to this work with: Behzad Amoozgar, Xiaoling Wei

    Affiliation Department of Biomedical Engineering, the University of Texas at Austin, Austin, Texas, United States of America

  • Jun Hui Lee,

    Affiliation Department of Ophthalmology, University of California, San Francisco, California, United States of America

  • Michele Bloomer,

    Affiliation Department of Ophthalmology, University of California, San Francisco, California, United States of America

  • Zhengtuo Zhao,

    Affiliation Department of Biomedical Engineering, the University of Texas at Austin, Austin, Texas, United States of America

  • Paul Coh,

    Affiliation Department of Ophthalmology, University of California, San Francisco, California, United States of America

  • Fei He,

    Affiliation Department of Biomedical Engineering, the University of Texas at Austin, Austin, Texas, United States of America

  • Lan Luan,

    Affiliation Department of Physics, the University of Texas at Austin, Austin, Texas, United States of America

  • Chong Xie , (YH); (CX)

    ‡ These authors also contributed equally to this work

    Affiliation Department of Biomedical Engineering, the University of Texas at Austin, Austin, Texas, United States of America

  • Ying Han (YH); (CX)

    ‡ These authors also contributed equally to this work

    Affiliation Department of Ophthalmology, University of California, San Francisco, California, United States of America

A novel flexible microfluidic meshwork to reduce fibrosis in glaucoma surgery

  • Behzad Amoozgar, 
  • Xiaoling Wei, 
  • Jun Hui Lee, 
  • Michele Bloomer, 
  • Zhengtuo Zhao, 
  • Paul Coh, 
  • Fei He, 
  • Lan Luan, 
  • Chong Xie, 
  • Ying Han



Fibrosis and hence capsule formation around the glaucoma implants are the main reasons for glaucoma implant failure. To address these issues, we designed a microfluidic meshwork and tested its biocompatibility in a rabbit eye model. The amount of fibrosis elicited by the microfluidic meshwork was compared to the amount elicited by the plate of conventional glaucoma drainage device.


Six eyes from 3 New Zealand albino rabbits were randomized to receive either the novel microfluidic meshwork or a plate of Ahmed glaucoma valve model PF7 (AGV PF7). The flexible microfluidic implant was made from negative photoresist SU-8 by using micro-fabrication techniques. The overall size of the meshwork was 7 mm × 7 mm with a grid period of 100 μm. Both implants were placed in the subtenon space at the supratemporal quadrant in a standard fashion. There was no communication between the implants and the anterior chamber via a tube. All animal eyes were examined for signs of infection and implant erosion on days 1, 3, 7, and 14 and then monthly. Exenterations were performed in which the entire orbital contents were removed at 3 months. Histology slides of the implant and the surrounding tissues were prepared and stained with hematoxylin-eosin. Thickness of the fibrous capsules beneath the implants were measured and compared with paired student’s t-test between the two groups.


The gross histological sections showed that nearly no capsule formed around the microfluidic meshwork in contrast to the thick capsule formed around the plate of AGV PF7. Thickness of the fibrotic capsules beneath the AGV PF7 plate from the 3 rabbit eyes was 90μm, 82μm, and 95 μm, respectively. The thickness at the bottom of fibrotic capsules around the new microfluidic implant were 1μm, 2μm, and 1μm, respectively. The difference in thickness of capsule between the two groups was significant (P = 0.002). No complications were noticed in the 6 eyes, and both implants were tolerated well by all rabbits.


The microfluidic meshwork elicited minimal fibrosis and capsule formation after 3-months implantation in a rabbit model. This provides promising evidence to aid in future development of a new glaucoma drainage implant that will elicit minimal scar formation and provide better long-term surgical outcomes.


Glaucoma is the leading cause of irreversible blindness in the world.[1] To date, controlling intraocular pressure (IOP) remains the primary treatment option. [2] Glaucoma surgery is commonly considered when glaucoma eye drops and laser therapies fail to lower IOP. [3]The fundamental concept of glaucoma surgery is to artificially create an additional pathway for aqueous humor (AH) outflow, therefore lowering IOP.

Trabeculectomy, glaucoma drainage implants (GDIs) and minimally invasive glaucoma surgeries (MIGS) are the currently available surgical treatment for glaucoma. Trabeculectomy is the standard surgical approach to treat adult primary glaucoma, but its success in children and certain glaucoma populations is limited.[47] GDIs were developed to treat patients with secondary glaucoma, pediatric glaucoma, and refractory glaucoma after failed trabeculectomy. Unfortunately, the long-term outcome of GDIs has not been satisfactory, largely due to fibrotic encapsulation of the implant that impedes the drainage of fluid.[8,9] MIGS is a relatively new approach with a superior safety profile, but mainly targets mild to moderate glaucoma with the goal of reducing the use of glaucoma drops. Failure, for all three types of glaucoma surgeries, results from the natural healing process of the human body that attempts to repair and close the new openings either at episcleral tissue for trabeculectomy [10,11] or around the implants for GDIs [1214] or MIGS.[15]

Thus, there is a critical need to develop an implant that can sustain the aqueous outflow while preventing obstruction due to fibrosis–the key to long-term functionality. Here, we present the concept for a modified GDI (Fig 1). The device design is based on that of the conventional GDI, however, we replaced the solid plate with a microfluidic meshwork in the fluid drainage region. The design of the meshwork was inspired by recently developed brain implants that can suppress chronic foreign body reactions.[16] We have incorporated two key features of the brain implants into the microfluidic meshwork design. Firstly, it consists of interconnected, cellular-dimensioned microfluidic channels that can conduct fluid. Secondly, it is ultra-flexible and conforms to the curvature and movement of the eye tissue after implantation. We hypothesize that these two features combined minimize fibrotic tissue formation around the meshwork, and therefore reduce the risk of failure of the drainage implants. In this work, as the initial test of the viability of this concept, we investigated the chronic tissue reactions to the implanted microfluidic meshwork alone where no tube was connected to the meshwork in the rabbit model. We used the plate of the conventional GDI, Ahmed glaucoma valve (AGV, PF7 model), as the control.

Fig 1. Proposed concept of a new GDI.

Plate of the GDI is replaced by the microfluidic meshwork.

Material and methods

Meshwork fabrication

The drainage devices were fabricated using photolithography techniques similar to those that were demonstrated previously.[17] The fabrication was done on silicon wafers with a nickel-releasing layer. Briefly, microchannel walls were patterned with negative photoresist SU-8 and the microchannels were formed by sacrificial photoresist (LOR 5A and AZ1505, Microchem, Westborough, MA). The meshwork had an overall area of 7mm × 7mm and a grid period of 100μm. The thickness of the meshwork was 4 μm (Fig 2). The microfluidic channels had outer diameters of 20 μm and inner diametersof 8μm. These parameters were determined according to finite element simulations to provide sufficient AH outflow (2 μL/min at 10 mmHg). After being released from the substrate, the meshworks were washed and stored in buffer solution prior to autoclave and implantation. The design, fabrication and simulation of the meshwork is documented elsewhere in details.[18]

Fig 2. Images of the microfluidic meshwork.

A. on a substrate. B. Zoom-in view of the mesh grids. Arrows denote the fluid outlets. Scale bars: 500 μm and 100 μm.

Animal preparation and standard surgical implantation

Three healthy Albino New Zealand rabbits (12–14 weeks old, and weighing 2–3 kg) were purchased and maintained at the Laboratory Animal Resource Center (LARC) at the University of California, San Francisco (UCSF). The Institutional Animal Care and Use Committee (IACUC) of UCSF approved the study. All animals were treated in accordance with the ARVO Statement for the Use of Animals in Ophthalmic and Vision Research. For each rabbit, the eyes were randomized to have one assigned to the current AGV PF7 silicone plate (no tube connected) and the other to the microfluidic meshwork (Fig 3). The surgery was performed in standard fashion in the animal microsurgery suite at UCSF. Under an operating microscope, the rabbits were anesthetized using an intramuscular injection of a mixture of ketamine hydrochloride (50 mg/kg) and xylazine hydrochloride (10 mg/kg), followed by mask anesthesia of isoflurane (2–4%). All efforts were made to minimize suffering of the animals. Both eyes were then prepared with povidone-iodine. For each eye, 6–0 Vicryl suture was passed through the supratemporal limbus to rotate the eye downward. Conjunctival peritomy was performed at the limbus in the supratemporal quadrant, followed by posterior dissection in the same plane. The flexible microfluidic meshwork was placed without suture and the AGV FP7 plate was sutured with 9–0 nylon sutures onto the episcleral surface approximately 6 mm from the limbus. The conjunctiva was closed with interrupted 8–0 vicryl sutures. There was no communication with the anterior chamber with either implant. To facilitate visualization of the microfluidic meshwork, a limbal 10–0 nylon suture was placed at the middle of the microfluidic meshwork. At the end of the surgery, subconjunctival cefazolin 0.1ml was given for antimicrobial prophylaxis. As routine postoperative care, the rabbit eyes were treated with Polymyxin antibiotic drops for one week and prednisolone acetate 1% drops starting with 3 times a day and then tapered every 3 days. All animal eyes were examined for signs of infection and plate erosion on days 1, 3, 7, and 14 and monthly thereafter for up to 3 months. Three months after surgery, the rabbits were euthanized by intravenous injection of potassium chloride or sodium pentobarbital after being anesthetized by isoflurane or ketamine/xylazine combination.

Fig 3. Implantation in rabbit eyes.

One eye was assigned to the conventional AGV PF7 silicone plate and the other to the microfluidic meshwork. No tube was connected with either AGV PF7 plate or the microfluidic meshwork.

Histology preparation

Three months after surgery, the rabbits were sacrificed and exenterations were performed in which the entire orbital contents were removed. Precautions were taken not to disturb the implants. After being fixed with 10% formalin, the eyes were dissected. Histology slides of the implant and the surrounding tissues were prepared and stained with hematoxylin-eosin (HE). The histological sections were examined and measured using light microscopy by a pathologist who was blinded to the different groups. Capsule thickness at the bottom of the plate was measured for each eye.

Statistical considerations

Paired student’s t-test was applied to compare the difference in the thickness of fibrous capsule between the microfluidic meshwork and conventional AGV PF7 plate groups. The rate of infection/plate erosion and any other notable side effects were compared between the two groups using the Fisher exact test.


Six eyes from 3 New Zealand rabbits underwent implantation of the plate of AGV PF7 in one eye and the microfluidic meshwork in the other in a randomized fashion. Two left eyes and one right eye received AGV PF7 while the other two right eyes and one left eye received the microfluidic meshwork. There was no tube connected to either AGV PF7 or the microfluidic meshwork. No significant complications were noticed during the implantation of both AGV PF7 and the microfluidic meshwork.

During the postoperative visits, there were no signs of infections, inflammation or erosion in any eye. All rabbits tolerated both types of implants well. After 3 months, exenterations were performed and the entire orbits were processed for HE staining. As shown in Fig 4, we observed that a thick capsule had formed around the plate of the AGV PF7 while nearly no capsule formed around the microfluidic meshwork (brown). Average thickness of the fibrotic capsules beneath the AGV PF7 and the microfluidic meshworks were 89 ± 6.6μm and 1.3 ± 0.6μm, respectively. There was a significant difference between the two groups (P = 0.002, Fig 5).

Fig 4. Gross section of tissue reactions to the microfluidic meshwork in comparison with AGV 3 months post implantation.

A. AGV B. microfluidic meshwork. Inset figures are magnified views of the microfluidic meshwork.

Fig 5. Histological study of tissue reaction to the microfluidic meshwork in comparison with AGV 3 months post implantation.

A. capsule beneath the plate of AGV; B. minimal reaction to the meshwork in rabbit 1, inset figure is a magnified view to a single channel of the meshwork (400x); C. minimal reaction to the meshwork in rabbit 2; D. minimal reaction to the meshwork in rabbit 3. Arrows in B, C and D is to delineate the meshwork.

During further inspection of all the histological slides of meshwork implants, we noticed that some inflammatory cells accumulated in the region where the meshwork had stacked into multiple layers during surgery (< 10% of the total area, Fig 6). This was not observed around monolayer meshwork.

Fig 6. Histological study of tissue reaction to the stacked microfluidic meshwork.

In the region where the meshwork has stacked into multiple layers during surgery, increased inflammatory reaction was noticed compared to the single layer region.


We presented here a modified concept of a GDI, in which the traditional plate of the GDI would be replaced by microfluidic meshwork. In this study, we tested our hypothesis that a properly designed meshwork can significantly suppress fibrotic tissue formation. In clear contrast to conventional implants, the microfluidic meshwork demonstrated excellent biocompatibility, evidenced by nearly no scar tissue and minimal inflammation.

Scar formation is the key obstacle in the surgical management of glaucoma. Modifications to the surgical technique as well as addition of intraoperative and postoperative medications have been studied in an effort to modulate fibrosis and promote long-term success with variable results.[1927] Mitomycin-C and 5-fluorouracil have been used intraoperatively and postoperatively to reduce inflammation.[19] However, the use of these agents has been associated with significant complications.[20,21] While corticosteroids offer reduced side effects, they are less potent and fail to provide significant improvement in long-term IOP reduction.[26] Modifications to the material comprising glaucoma surgical devices have also been explored. Studies that compared conventional silicone flexible GDI with polypropylene rigid GDI have shown a lower rate of encapsulation and higher success rates with the flexible plate.[28] Several novel designs of glaucoma surgical devices aimed at reducing scar formation have been tested, including a MMC-coated valve, Ferrofluid valve, expanded polytetrafluoroethylene enclosed Ahmed, and Ahmed Glaucoma Valve with Adjunctive Amniotic Membrane.[2932] These modifications and designs have been shown to decrease the amount of fibrosis and scar tissue when compared to conventional glaucoma devices but still resulted in significant capsule formation.[31,32]

The most active phase of capsule formation occurs in the 3 months following implantation.[8] Although many theories have been proposed to explain the increased rate of encapsulation with glaucoma surgical devices, including those on the physical profile of the implant (e.g. size and material) and fibrosis stimulation through early exposure to inflammatory mediators,[28,33,34] the fundamental mechanisms of these tissue reactions are not clearly understood. Nonetheless, in a series of recent works,[35] neural probes were successfully engineered to suppress tissue reactions by addressing two important problems. First, the mechanical mismatch between the tissue and the implant gives rise to interfacial forces that constantly elicit tissue reactions. Second, the presence of the solid implant interrupts the cellular and vascular networks at the implant site.[9] In order to achieve optimal biocompatibility, these two issues must be addressed through substantial changes to the implant’s mechanical properties and geometric structure. Hence, the implant was designed as a network of ultra-flexible interconnected cellular-sized channels in order to optimize its fluidic conductance while introducing minimum perturbation to the cellular and vascular processes at the implant site.

Additionally, during the histological examination of the dissected specimens, we noticed some inflammatory cell activation at the edge of the meshwork implant wherever the meshwork was folded or stacked into layers during the surgery. These regions were less than 10% of the total meshwork area. We postulated that when the meshwork was folded into multiple layers, its flexibility and hence its biocompatibility with eye tissue was compromised. This led to increased inflammatory cell activation and aggregation. This was not noticed in the majority of the areas where a single layer was maintained.

We chose a New Zealand rabbit model for this study because this model has been previously used to study the effects of various biomaterials as well as newly-designed glaucoma surgical devices on the degree of fibrosis.[36,37] Subsequent clinical studies were concordant and confirmed the applicability of the rabbit model.[23,38] The plate of AGV FP7, one of the most commonly used glaucoma surgical device in practice, was chosen as the control group. In addition to its popularity, AGV FP7 has been well characterized in the rabbit model and a large amount of published histological results can serve as reference. In our study, the average capsule thickness under the AGV PF7 plate implant was 89μm, which is comparable with the capsule thickness reported in the literature.[2932]

One limitation of this study was that we only studied the tissue reactions to non-fluid draining implants. The mechanical mismatch between tissue and implant may not be the only factor affecting fibrosis. It is known that inflamed AH may also lead to inflammation around the implant and elicit tissue reactions,[39] and this study does not account for this. However, our results show that the AGV PF7 plate had a significant amount of fibrotic capsule even without AH flow. This suggests that the implant itself is one of the major, if not the total, cause of fibrosis. Furthermore, inflamed AH can be treated with extensive anti-inflammatory medication, such as steroid eye drops and/or anti-aqueous suppressants to minimize the effect. In the next step, we plan to construct a complete GDI from the microfluidic meshwork and investigate its fluidic dynamics as well as tissue reactions while accounting for the AH flow.

In summary, this study demonstrated that the flexible microfluidic meshwork elicited minimal scar formation after being implanted into rabbit eyes for 3 months. We believe that these encouraging results warrant further development of a new GDI based on the microfluidic meshwork. The resulting GDI may significantly reduce fibrosis around the device and improve long-term success rates of glaucoma surgery across the spectrum.


This study is a collaborative effort between the scientists from UCSF Medical Center, Department of Ophthalmology, University of Texas at Austin, Department of Physics and University of Texas at Austin Department of Biomedical Engineering along with the IACUC veterinary staff at UCSF.

Author Contributions

  1. Conceptualization: CX YH XW FH ZZ LL.
  2. Data curation: CX YH XW FH ZZ LL.
  3. Formal analysis: CX YH XW FH ZZ LL.
  4. Funding acquisition: CX YH.
  5. Investigation: BA CX YH XW FH ZZ LL MB.
  6. Methodology: CX YH XW FH ZZ LL.
  7. Project administration: BA PC CX YH XW FH ZZ LL.
  8. Resources: BA CX YH XW FH ZZ LL.
  9. Software: CX YH XW FH ZZ LL.
  10. Supervision: CX YH.
  11. Validation: CX YH MB.
  12. Visualization: CX YH BA JHL PC MB.
  13. Writing – original draft: CX YH BA JHL PC.
  14. Writing – review & editing: CX YH BA JHL PC.


  1. 1. Vajaranant TS, Wu S, Torres M, Varma R. The changing face of primary open-angle glaucoma in the United States: demographic and geographic changes from 2011 to 2050. Am J Ophthalmol 2012;154(2):303–314. e3. pmid:22541661
  2. 2. Caprioli J, Varma R. Intraocular pressure: modulation as treatment for glaucoma. Am J Ophthalmol 2011;152(3):340–344. e2. pmid:21855671
  3. 3. Lama PJ, Fechtner RD. Antifibrotics and wound healing in glaucoma surgery. Surv Ophthalmol 2003;48(3):314–346. pmid:12745005
  4. 4. Tanimoto SA, Brandt JD. Options in pediatric glaucoma after angle surgery has failed. Curr Opin Ophthalmol 2006 Apr;17(2):132–137. pmid:16552247
  5. 5. Gressel MG, Heuer DK, Parrish RK. Trabeculectomy in young patients. Ophthalmology 1984;91(10):1242–1246. pmid:6083518
  6. 6. Iwao K, Inatani M, Seto T, Takihara Y, Ogata-Iwao M, Okinami S, et al. Long-term outcomes and prognostic factors for trabeculectomy with mitomycin C in eyes with uveitic glaucoma: a retrospective cohort study. J Glaucoma 2014 Feb;23(2):88–94. pmid:22895522
  7. 7. Takihara Y, Inatani M, Seto T, Iwao K, Iwao M, Inoue T, et al. Trabeculectomy with mitomycin for open-angle glaucoma in phakic vs pseudophakic eyes after phacoemulsification. Arch Ophthalmol 2011;129(2):152–157. pmid:21320958
  8. 8. Thieme H, Choritz L, Hofmann-Rummelt C, Schloetzer-Schrehardt U, Kottler UB. Histopathologic findings in early encapsulated blebs of young patients treated with the ahmed glaucoma valve. J Glaucoma 2011 Apr-May;20(4):246–251. pmid:20520569
  9. 9. Foreign body reaction to biomaterials. Seminars in immunology: Elsevier; 2008.
  10. 10. Yamanaka O, Kitano-Izutani A, Tomoyose K, Reinach PS. Pathobiology of wound healing after glaucoma filtration surgery. BMC ophthalmology 2015;15(1):19.
  11. 11. Van de Velde S, Van Bergen T, Vandewalle E, Moons L, Stalmans I. Modulation of wound healing in glaucoma surgery. Prog Brain Res 2015;221:319–340. pmid:26518085
  12. 12. Danesh-Meyer HV, Spaeth GL, Maus M. Cosmetically significant proptosis following a tube shunt procedure. Arch Ophthalmol 2002;120(6):846–847. pmid:12049596
  13. 13. Gedde SJ, Schiffman JC, Feuer WJ, Herndon LW, Brandt JD, Budenz DL, et al. Treatment outcomes in the Tube Versus Trabeculectomy (TVT) study after five years of follow-up. Am J Ophthalmol 2012;153(5):789–803. e2. pmid:22245458
  14. 14. Budenz DL, Barton K, Gedde SJ, Feuer WJ, Schiffman J, Costa VP, et al. Five-year treatment outcomes in the Ahmed Baerveldt comparison study. Ophthalmology 2015;122(2):308–316. pmid:25439606
  15. 15. Brandao LM, Grieshaber MC. Update on Minimally Invasive Glaucoma Surgery (MIGS) and New Implants. J Ophthalmol 2013;2013:705915. pmid:24369494
  16. 16. Xie C, Liu J, Fu T, Dai X, Zhou W, Lieber CM. Three-dimensional macroporous nanoelectronic networks as minimally invasive brain probes. Nature materials 2015;14(12):1286–1292. pmid:26436341
  17. 17. Liu J, Xie C, Dai X, Jin L, Zhou W, Lieber CM. Multifunctional three-dimensional macroporous nanoelectronic networks for smart materials. Proc Natl Acad Sci U S A 2013 Apr 23;110(17):6694–6699. pmid:23569270
  18. 18. Wei X, Lee J, H., Zhao Z, Amoozgar B, He F, Bloomer M, et al. Ultra-flexible Microfluidic Meshwork for Minimally Invasive Glaucoma Surgery. Forthcoming.
  19. 19. Alvarado JA, Hollander DA, Juster RP, Lee LC. Ahmed valve implantation with adjunctive mitomycin C and 5-fluorouracil: long-term outcomes. Am J Ophthalmol 2008;146(2):276–284. e2. pmid:18538300
  20. 20. Costa VP, Azuara-Blanco A, Netland PA, Lesk MR, Arcieri ES. Efficacy and safety of adjunctive mitomycin C during Ahmed Glaucoma Valve implantation: a prospective randomized clinical trial. Ophthalmology 2004;111(6):1071–1076. pmid:15177955
  21. 21. Yazdani S, Mahboobipour H, Pakravan M, Doozandeh A, Ghahari E. Adjunctive Mitomycin C or Amniotic Membrane Transplantation for Ahmed Glaucoma Valve Implantation: A Randomized Clinical Trial. J Glaucoma 2016 May;25(5):415–421. pmid:25967528
  22. 22. Pakravan M, Rad SS, Yazdani S, Ghahari E, Yaseri M. Effect of early treatment with aqueous suppressants on Ahmed glaucoma valve implantation outcomes. Ophthalmology 2014;121(9):1693–1698. pmid:24819857
  23. 23. Law SK, Nguyen A, Coleman AL, Caprioli J. Comparison of safety and efficacy between silicone and polypropylene Ahmed glaucoma valves in refractory glaucoma. Ophthalmology 2005;112(9):1514–1520. pmid:16005977
  24. 24. Kurnaz E, Kubaloglu A, Yilmaz Y, Koytak A, Ozerturk Y. The effect of adjunctive Mitomycin C in Ahmed glaucoma valve implantation. Eur J Ophthalmol 2005;15(1):27–31.
  25. 25. Susanna R. Partial Tenon's Capsule Resection with Adjunctive Mitomicyn C in Ahmed Glaucoma Valve Insertion. Invest Ophthalmol Vis Sci 2003;44(13):1181–1181.
  26. 26. Teixeira SH, Doi LM, Freitas Silva AL, Silva KD, Paes AT, Higa FS, et al. Silicone Ahmed glaucoma valve with and without intravitreal triamcinolone acetonide for neovascular glaucoma: randomized clinical trial. J Glaucoma 2012 Jun-Jul;21(5):342–348. pmid:21423036
  27. 27. Turalba AV, Pasquale LR. Hypertensive phase and early complications after Ahmed glaucoma valve implantation with intraoperative subtenon triamcinolone acetonide. Clin Ophthalmol 2014 Jul 11;8:1311–1316. pmid:25050061
  28. 28. Hinkle D, Zurakowski D, Ayyala R. A comparison of the polypropylene plate AhmedTM glaucoma valve to the silicone plate AhmedTM glaucoma flexible valve. Eur J Ophthalmol 2007;17(5):696–701. pmid:17932842
  29. 29. Sahiner N, Kravitz DJ, Qadir R, Blake DA, Haque S, John VT, et al. Creation of a drug-coated glaucoma drainage device using polymer technology: in vitro and in vivo studies. Arch Ophthalmol 2009;127(4):448–453. pmid:19365022
  30. 30. Paschalis EI, Chodosh J, Sperling RA, Salvador-Culla B, Dohlman C. A novel implantable glaucoma valve using ferrofluid. PloS one 2013;8(6):e67404. pmid:23840691
  31. 31. DeCroos FC, Ahmad S, Kondo Y, Chow J, Mordes D, Lee MR, et al. Expanded polytetrafluoroethylene membrane alters tissue response to implanted Ahmed glaucoma valve. Curr Eye Res 2009;34(7):562–567. pmid:19899969
  32. 32. Lee JW, Park WY, Kim EA, Yun IH. Tissue response to implanted Ahmed glaucoma valve with adjunctive amniotic membrane in rabbit eyes. Ophthalmic Res 2014;51(3):129–139. pmid:24503529
  33. 33. Nouri-Mahdavi K, Caprioli J. Evaluation of the hypertensive phase after insertion of the Ahmed glaucoma valve. Am J Ophthalmol 2003;136(6):1001–1008. pmid:14644209
  34. 34. Gedde SJ, Panarelli JF, Banitt MR, Lee RK. Evidenced-based comparison of aqueous shunts. Curr Opin Ophthalmol 2013 Mar;24(2):87–95. pmid:23287104
  35. 35. Liu J, Fu TM, Cheng Z, Hong G, Zhou T, Jin L, et al. Syringe-injectable electronics. Nat Nanotechnol 2015 Jul;10(7):629–636. pmid:26053995
  36. 36. Ayyala RS, Harman LE, Michelini-Norris B, Ondrovic LE, Haller E, Margo CE, et al. Comparison of different biomaterials for glaucoma drainage devices. Arch Ophthalmol 1999;117(2):233–236. pmid:10037569
  37. 37. Ayyala RS, Michelini-Norris B, Flores A, Haller E, Margo CE. Comparison of different biomaterials for glaucoma drainage devices: part 2. Arch Ophthalmol 2000;118(8):1081–1084. pmid:10922202
  38. 38. Ishida K, Netland PA, Costa VP, Shiroma L, Khan B, Ahmed IIK. Comparison of polypropylene and silicone Ahmed glaucoma valves. Ophthalmology 2006;113(8):1320–1326. pmid:16877071
  39. 39. Kim YG, Hong S, Lee CS, Kang SY, Seong GJ, Ma KT, et al. Level of vascular endothelial growth factor in aqueous humor and surgical results of ahmed glaucoma valve implantation in patients with neovascular glaucoma. J Glaucoma 2009 Aug;18(6):443–447. pmid:19680051